Home 
How Blumble Works 
Search Algorithm 
Your Privacy 
About 
Facebook
Twitter
Blog
Most recent job postings at Vivo
via Dice
posted_at: 2 days agoschedule_type: Full-time
Piper Companies is currently looking for an experienced In-Vivo Program manager in Philadelphia, Pennsylvania (PA) to work for an innovative and growing pharmaceutical company. The In-Vivo Program Manager will play an integral part in overseeing vendor relationships related to clinical research into immunological pharmaceutical products.
Responsibilities for the In-Vivo Program manager... include:
• Participate in design of experiment (DOE) of
Piper Companies is currently looking for an experienced In-Vivo Program manager in Philadelphia, Pennsylvania (PA) to work for an innovative and growing pharmaceutical company. The In-Vivo Program Manager will play an integral part in overseeing vendor relationships related to clinical research into immunological pharmaceutical products.
Responsibilities for the In-Vivo Program manager... include:
• Participate in design of experiment (DOE) of clinical studies related to immunological pharmaceutical research
• Act as a subject matter expert to the study troubleshooting potential vendor issues
• Oversee vendor management and act as main point of contact to external vivarium's and CRO's
• Oversee the transportation of samples, and animal tissue from external vendors to internal laboratories
• Complete and process laboratory/logistical documentation and perform database maintenance utilizing Microsoft Word, Excel & Access programs.
Qualifications for the In-Vivo Program manager include:
• 2-3 years of hands-on experience overseeing In-Vivo studies within a pharmaceutical organization or CRO
• Hands on experience with mouse model development including the assessment of pharmacodynamic effects of drug candidates in vivo
• Holds a Ph.D. or Masters in Biomedical Science or related field
Compensation for the In-Vivo Program manager include:
• Salary Range is dependent upon experience
• Comprehensive benefits package
Keywords
In Vivo, Program Manager, Immunology, Vendor Management, Philadelphia, PA, Pennsylvania, Research, Science, comprehensive benefits package, Health, Vision, Dental Show more details...
Responsibilities for the In-Vivo Program manager... include:
• Participate in design of experiment (DOE) of clinical studies related to immunological pharmaceutical research
• Act as a subject matter expert to the study troubleshooting potential vendor issues
• Oversee vendor management and act as main point of contact to external vivarium's and CRO's
• Oversee the transportation of samples, and animal tissue from external vendors to internal laboratories
• Complete and process laboratory/logistical documentation and perform database maintenance utilizing Microsoft Word, Excel & Access programs.
Qualifications for the In-Vivo Program manager include:
• 2-3 years of hands-on experience overseeing In-Vivo studies within a pharmaceutical organization or CRO
• Hands on experience with mouse model development including the assessment of pharmacodynamic effects of drug candidates in vivo
• Holds a Ph.D. or Masters in Biomedical Science or related field
Compensation for the In-Vivo Program manager include:
• Salary Range is dependent upon experience
• Comprehensive benefits package
Keywords
In Vivo, Program Manager, Immunology, Vendor Management, Philadelphia, PA, Pennsylvania, Research, Science, comprehensive benefits package, Health, Vision, Dental Show more details...
via Science Careers
posted_at: 5 days agoschedule_type: Full-time
The Senior Research Associate will be responsible for overseeing and performing in vivo studies to support the ocular therapeutic area and all the therapeutic areas of the translational team.
• Perform Ocular in vivo studies to support in support of Spark pipeline.
• Perform Intravitreal/Subretinal injections, monitor animal health, collect blood samples, perform necropsies and record data for... mouse studies, other species as needed.
• Perform
The Senior Research Associate will be responsible for overseeing and performing in vivo studies to support the ocular therapeutic area and all the therapeutic areas of the translational team.
• Perform Ocular in vivo studies to support in support of Spark pipeline.
• Perform Intravitreal/Subretinal injections, monitor animal health, collect blood samples, perform necropsies and record data for... mouse studies, other species as needed.
• Perform Electroretinography, OCT and OKR monitoring in rodents.
• Maintain rodent breeding colonies.
• Perform IV/IP/PO/SC injections in mice and rats.
• General supplies and reagent ordering.
• Interact with ocular scientists and provide constant feedback.
• Work cross-functionally with CNS, and liver teams and support other R&D in vivo teams as needed.
• Schedule and follow multiple concurrent studies according to the experimental design.
• Interact with scientists of different therapeutic areas and provide constant feedback.
Responsibilities
% of Time
Job Function and Description
50%
Perform Ocular in vivo experiments in laboratory animals according to applicable regulations; studies will utilize mice and also rats, rabbits and other species, as needed
20%
Train and assist technical staff in the performance of in vivo experiments to support ocular and other therapeutic areas.
Responsible for all safety aspects and best practices, and employee training.
Ensure departmental goals and objectives are met and aligned to the broader organizational goals and objectives.
30%
Prioritize and plan projects and workloads, manage resources and personnel scheduling. Write and review animal protocols for IACUC approval
Education and Experience Requirements
• Bachelor’s degree/MS in relevant field required and 5+ years of hands on experience with rodents.
• Advanced skills on handling, restraining, dosing and performing a variety of procedures on study animals required.
• Ability to manage large mouse colonies required.
• Excellent organizational, communication and collaboration skills.
• Keep accurate records, follow instructions and comply with company policies.
• Experience with AAV vectors is a plus.
• Micro-surgical techniques preferred
Key Skills, Abilities, and Competencies
• Strong organizational skills.
• Excellent writing and verbal communication skills.
• Proficiency
Complexity and Problem Solving
• Demonstrate independent problem solving skills of technical issues; develop solutions to a variety of moderate to complex problems; Discuss with supervisor and refer to policies/practices for guidance.
• Must be comfortable in the fast-paced, biotech start-up environment and interact with multi-disciplinary research teams at Spark.
• Exercise judgment within defined procedures and practices to determine appropriate action.
Internal and External Contacts
Quality Assurance, Technology & Research Operations, Pharm/Tox, Discovery, Bioanalytics Operations, Technical Operations, Regulatory Affairs
Please be aware that Spark mandates COVID-19 vaccination of all employees regardless of work location. Accommodations may be made in accordance with applicable law.
Spark Therapeutics does not accept unsolicited resumes/candidate profiles from any source other than directly from candidates. Any unsolicited resume/candidate profile submitted through our website or to personal email accounts of employees of Spark Therapeutics are considered property of Spark Therapeutics and are not subject to payment of agency fees.
Nearest Major Market: Philadelphia
Join the Spark Team
We were born of innovation, springing from the curiosity, imagination and dedication of remarkable scientists and healthcare visionaries. Our shared mission is to challenge the inevitability of genetic disease by discovering, developing, and delivering treatments in ways unimaginable - until now.
We don't follow footsteps. We create the path.
Learn more about Spark Therapeutics and view other openings Show more details...
• Perform Ocular in vivo studies to support in support of Spark pipeline.
• Perform Intravitreal/Subretinal injections, monitor animal health, collect blood samples, perform necropsies and record data for... mouse studies, other species as needed.
• Perform Electroretinography, OCT and OKR monitoring in rodents.
• Maintain rodent breeding colonies.
• Perform IV/IP/PO/SC injections in mice and rats.
• General supplies and reagent ordering.
• Interact with ocular scientists and provide constant feedback.
• Work cross-functionally with CNS, and liver teams and support other R&D in vivo teams as needed.
• Schedule and follow multiple concurrent studies according to the experimental design.
• Interact with scientists of different therapeutic areas and provide constant feedback.
Responsibilities
% of Time
Job Function and Description
50%
Perform Ocular in vivo experiments in laboratory animals according to applicable regulations; studies will utilize mice and also rats, rabbits and other species, as needed
20%
Train and assist technical staff in the performance of in vivo experiments to support ocular and other therapeutic areas.
Responsible for all safety aspects and best practices, and employee training.
Ensure departmental goals and objectives are met and aligned to the broader organizational goals and objectives.
30%
Prioritize and plan projects and workloads, manage resources and personnel scheduling. Write and review animal protocols for IACUC approval
Education and Experience Requirements
• Bachelor’s degree/MS in relevant field required and 5+ years of hands on experience with rodents.
• Advanced skills on handling, restraining, dosing and performing a variety of procedures on study animals required.
• Ability to manage large mouse colonies required.
• Excellent organizational, communication and collaboration skills.
• Keep accurate records, follow instructions and comply with company policies.
• Experience with AAV vectors is a plus.
• Micro-surgical techniques preferred
Key Skills, Abilities, and Competencies
• Strong organizational skills.
• Excellent writing and verbal communication skills.
• Proficiency
Complexity and Problem Solving
• Demonstrate independent problem solving skills of technical issues; develop solutions to a variety of moderate to complex problems; Discuss with supervisor and refer to policies/practices for guidance.
• Must be comfortable in the fast-paced, biotech start-up environment and interact with multi-disciplinary research teams at Spark.
• Exercise judgment within defined procedures and practices to determine appropriate action.
Internal and External Contacts
Quality Assurance, Technology & Research Operations, Pharm/Tox, Discovery, Bioanalytics Operations, Technical Operations, Regulatory Affairs
Please be aware that Spark mandates COVID-19 vaccination of all employees regardless of work location. Accommodations may be made in accordance with applicable law.
Spark Therapeutics does not accept unsolicited resumes/candidate profiles from any source other than directly from candidates. Any unsolicited resume/candidate profile submitted through our website or to personal email accounts of employees of Spark Therapeutics are considered property of Spark Therapeutics and are not subject to payment of agency fees.
Nearest Major Market: Philadelphia
Join the Spark Team
We were born of innovation, springing from the curiosity, imagination and dedication of remarkable scientists and healthcare visionaries. Our shared mission is to challenge the inevitability of genetic disease by discovering, developing, and delivering treatments in ways unimaginable - until now.
We don't follow footsteps. We create the path.
Learn more about Spark Therapeutics and view other openings Show more details...
via Salary.com
posted_at: 13 days agoschedule_type: Full-time
Qualifications Include:
• Bachelor of Architecture Degree
• 10 years of experience. Previous experience in the Life Sciences...
industry preferred
• Registered or working toward an architectural registration is a plus
• Strong Revit and AutoCAD skills
• Experience with design presentation programs such as Sketch-up,
Enscape, and Photoshop;
• Management of Construction Document development
• Understanding of Construction Detailing and
Qualifications Include:
• Bachelor of Architecture Degree
• 10 years of experience. Previous experience in the Life Sciences...
industry preferred
• Registered or working toward an architectural registration is a plus
• Strong Revit and AutoCAD skills
• Experience with design presentation programs such as Sketch-up,
Enscape, and Photoshop;
• Management of Construction Document development
• Understanding of Construction Detailing and Building Codes
• Self-motivated – ability to work independently, as well as collaborate
as a team member
• Detail-oriented – ability to perform self as well as peer review of drawings
Resumes should be sent to Matthew O'Brien at mobrien@vivoarch.co Show more details...
• Bachelor of Architecture Degree
• 10 years of experience. Previous experience in the Life Sciences...
industry preferred
• Registered or working toward an architectural registration is a plus
• Strong Revit and AutoCAD skills
• Experience with design presentation programs such as Sketch-up,
Enscape, and Photoshop;
• Management of Construction Document development
• Understanding of Construction Detailing and Building Codes
• Self-motivated – ability to work independently, as well as collaborate
as a team member
• Detail-oriented – ability to perform self as well as peer review of drawings
Resumes should be sent to Matthew O'Brien at mobrien@vivoarch.co Show more details...
via Charles River - Charles River Laboratories
posted_at: 14 days agoschedule_type: Full-time
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we... perform. In return, we’ll help you build a career
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we... perform. In return, we’ll help you build a career that you can feel passionate about.
Job Summary
We are seeking an Operational Supervisor to join our Integrated Toxicology (ITox) team at the Kansas City (CR-KAN) Site. This site is the first of its kind, bridging CRL’s Discovery and Safety Assessment business units, while bringing automation to standard lead optimization toxicology study models to deliver rapid study results to our clients. When you join our family, you will have a significant impact on the health and well-being of people across the globe. This role will be responsible for the oversight of in-vivo operations staff and all daily functions to support animal care and study execution. They will provide, coordinate, document, and schedule routine and highly complex training activities for In-Life, Animal Care, and Cage Wash personnel. This individual will also be responsible for defining a new technical training plan, in alignment with the global program, that includes developing, revising, and implementing the use of training documents and processes. They will also provide leadership and mentor less experienced personnel as well as provide leadership and/or support of new hire orientation.
Job Qualifications
ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Provide guidance in the day-to-day activities of assigned departmental employees to ensure accurate, high-quality work, and adherence to pertinent departmental policies, practices, and procedures (SOPs, safety procedures and biosafety protocols). Ensure schedule is prepared daily, accurately reflecting required tasks and workload. Serve as a model as it relates to effective time management, communication, and utilization of resources.
• Perform technical tasks to support completion of study tasks (as needed).
• Lead and mentor less experienced training personnel.
• Work with department management to coordinate and facilitate multi-species technical training at all levels of complexity for department personnel.
• Maintain and update all documents and databases used for the support and conduct of training tasks, including but not limited to training standards, training records, training timelines, and proficiency standards.
• Provide oversight, scheduling, and coordination of training animal use to enable optimal learning while prioritizing animal care and welfare.
• Practice/maintain advanced technical skills and procedures, work independently, and follow operating procedures and processes.
• May conduct sponsor/visitor tours and interact with clients.
• Provide input/review of new, and/or revised processes, operating procedures, training standards, quizzes, proficiency standards, and other training documents.
• Assist in facilitating, coordinating, and scheduling new hire orientation and on-the-job training for personnel.
• Participate in recruiting efforts by assisting in interviews and selecting qualified non-exempt level departmental personnel.
• Assist in the scheduling, coordination, and execution of study procedures.
• 24/7 emergency duty coverage as assigned.
• Perform all other related duties as assigned.
QUALIFICATIONS:
• Education: Bachelor’s degree (B.A./B.S.) or equivalent in scientific related discipline.
• Experience: 4-6 years related experience in animal science, biology, chemistry/pharmacy, or similar lab environment.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Certification/Licensure: AALAS certification ALAT/LAT level strongly preferred; or other applicable certification/licensure.
• Other: Demonstrated advanced technical and analytical skills. Effective communication and leadership skills. Ability to handle a variety of laboratory animals. Proficient in technical skills and the operation of data collection equipment. Knowledge of GLPs and other federal regulations and guidelines relating to the care of laboratory animals required. Understanding of basic, intermediate, and complex study design and protocols. Ability to organize and prioritize work to meet deadlines. Computer literacy including word processing, spreadsheet, and database programs.
“The pay range for this position is $70,000+. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.”
About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.
About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.
Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit www.criver.com Show more details...
Job Summary
We are seeking an Operational Supervisor to join our Integrated Toxicology (ITox) team at the Kansas City (CR-KAN) Site. This site is the first of its kind, bridging CRL’s Discovery and Safety Assessment business units, while bringing automation to standard lead optimization toxicology study models to deliver rapid study results to our clients. When you join our family, you will have a significant impact on the health and well-being of people across the globe. This role will be responsible for the oversight of in-vivo operations staff and all daily functions to support animal care and study execution. They will provide, coordinate, document, and schedule routine and highly complex training activities for In-Life, Animal Care, and Cage Wash personnel. This individual will also be responsible for defining a new technical training plan, in alignment with the global program, that includes developing, revising, and implementing the use of training documents and processes. They will also provide leadership and mentor less experienced personnel as well as provide leadership and/or support of new hire orientation.
Job Qualifications
ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Provide guidance in the day-to-day activities of assigned departmental employees to ensure accurate, high-quality work, and adherence to pertinent departmental policies, practices, and procedures (SOPs, safety procedures and biosafety protocols). Ensure schedule is prepared daily, accurately reflecting required tasks and workload. Serve as a model as it relates to effective time management, communication, and utilization of resources.
• Perform technical tasks to support completion of study tasks (as needed).
• Lead and mentor less experienced training personnel.
• Work with department management to coordinate and facilitate multi-species technical training at all levels of complexity for department personnel.
• Maintain and update all documents and databases used for the support and conduct of training tasks, including but not limited to training standards, training records, training timelines, and proficiency standards.
• Provide oversight, scheduling, and coordination of training animal use to enable optimal learning while prioritizing animal care and welfare.
• Practice/maintain advanced technical skills and procedures, work independently, and follow operating procedures and processes.
• May conduct sponsor/visitor tours and interact with clients.
• Provide input/review of new, and/or revised processes, operating procedures, training standards, quizzes, proficiency standards, and other training documents.
• Assist in facilitating, coordinating, and scheduling new hire orientation and on-the-job training for personnel.
• Participate in recruiting efforts by assisting in interviews and selecting qualified non-exempt level departmental personnel.
• Assist in the scheduling, coordination, and execution of study procedures.
• 24/7 emergency duty coverage as assigned.
• Perform all other related duties as assigned.
QUALIFICATIONS:
• Education: Bachelor’s degree (B.A./B.S.) or equivalent in scientific related discipline.
• Experience: 4-6 years related experience in animal science, biology, chemistry/pharmacy, or similar lab environment.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Certification/Licensure: AALAS certification ALAT/LAT level strongly preferred; or other applicable certification/licensure.
• Other: Demonstrated advanced technical and analytical skills. Effective communication and leadership skills. Ability to handle a variety of laboratory animals. Proficient in technical skills and the operation of data collection equipment. Knowledge of GLPs and other federal regulations and guidelines relating to the care of laboratory animals required. Understanding of basic, intermediate, and complex study design and protocols. Ability to organize and prioritize work to meet deadlines. Computer literacy including word processing, spreadsheet, and database programs.
“The pay range for this position is $70,000+. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.”
About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.
About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.
Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit www.criver.com Show more details...
via CareerBuilder
posted_at: 3 days agoschedule_type: Full-time
Req Number 85381
Job Description...
RESPONSIBILITIES:-
• Assists Registered Pharmacist in the non-professional (non-judgmental) aspects preparing and dispensing medication.
• Fills, packages, labels and stocks unit dose cart from patient profile card or computerized pick list; brings cart to nursing unit according to predetermined schedule. Makes other deliveries, as required.
• Fills bottles or other package forms with measured amount of
Req Number 85381
Job Description...
RESPONSIBILITIES:-
• Assists Registered Pharmacist in the non-professional (non-judgmental) aspects preparing and dispensing medication.
• Fills, packages, labels and stocks unit dose cart from patient profile card or computerized pick list; brings cart to nursing unit according to predetermined schedule. Makes other deliveries, as required.
• Fills bottles or other package forms with measured amount of medication either manually or mechanically.
• Labels containers of drugs according to department specification, either manually or mechanically.
• Assists in clean air room, using sterile technique in filling and labeling injectable prescriptions, where required.
• Assists in preparation and/or labeling of IV additives.
• Fills medication orders in inpatient area.
• Packages sudden, unexpected medication requests, as required.
• Assists Registered Pharmacist in maintaining a variety of records and reports.
• Maintains IV records with Pharmacist direction.
• Maintains records for medication in inpatient area.
• Maintains records of preparation of extemporaneous medications.
• Assists in the maintenance of statistics and records for all medication orders.
• Enters orders into computer terminal for refill purposes.
• Maintains sufficient inventory at workstations in Pharmacy.
• Transports required pharmacy material, as necessary.
• Receives and maintains records of stock and inventory control.
• Assists in material control by maintaining records and inventories.
• Maintains placement of sufficient daily inventory of supplies to all areas of the Pharmacy to assure efficient operating conditions.
• Performs related duties, as required.
• ADA Essential Functions
EXPERIENCE AND QUALIFICATIONS
• High School Diploma or equivalent, required.
• Current national certification through Pharmacy Technician Certification Board (PTCB)/National Healthcare Association (NHA), required.
• NYSED- License
• Minimum of two (2) years experience as a Pharmacy Technician in a hospital pharmacy with a computerized system, preferred.
• Ability to learn computerized hospital pharmacy system.
Must be able to do physically strenuous work.
• Additional Salary Detail
The salary range and/or hourly rate listed is a good faith determination of potential base compensation that may be offered to a successful applicant for this position at the time of this job advertisement and may be modified in the future. When determining a team member's base salary and/or rate, several factors may be considered as applicable (e.g., location, specialty, service line, years of relevant experience, education, credentials, negotiated contracts, budget and internal equity).
The salary range for this position is $25-$25/hour
It is Northwell Health’s policy to provide equal employment opportunity and treat all applicants and employees equally regardless of their age, race, creed/religion, color, national origin, immigration status or citizenship status, sexual orientation, military or veteran status, sex/gender, gender identity, gender expression, disability, pregnancy, genetic information or genetic predisposition or carrier status, marital or familial status, partnership status, victim of domestic violence, sexual or other reproductive health decisions, or other characteristics protected by applicable law Show more details...
Job Description...
RESPONSIBILITIES:-
• Assists Registered Pharmacist in the non-professional (non-judgmental) aspects preparing and dispensing medication.
• Fills, packages, labels and stocks unit dose cart from patient profile card or computerized pick list; brings cart to nursing unit according to predetermined schedule. Makes other deliveries, as required.
• Fills bottles or other package forms with measured amount of medication either manually or mechanically.
• Labels containers of drugs according to department specification, either manually or mechanically.
• Assists in clean air room, using sterile technique in filling and labeling injectable prescriptions, where required.
• Assists in preparation and/or labeling of IV additives.
• Fills medication orders in inpatient area.
• Packages sudden, unexpected medication requests, as required.
• Assists Registered Pharmacist in maintaining a variety of records and reports.
• Maintains IV records with Pharmacist direction.
• Maintains records for medication in inpatient area.
• Maintains records of preparation of extemporaneous medications.
• Assists in the maintenance of statistics and records for all medication orders.
• Enters orders into computer terminal for refill purposes.
• Maintains sufficient inventory at workstations in Pharmacy.
• Transports required pharmacy material, as necessary.
• Receives and maintains records of stock and inventory control.
• Assists in material control by maintaining records and inventories.
• Maintains placement of sufficient daily inventory of supplies to all areas of the Pharmacy to assure efficient operating conditions.
• Performs related duties, as required.
• ADA Essential Functions
EXPERIENCE AND QUALIFICATIONS
• High School Diploma or equivalent, required.
• Current national certification through Pharmacy Technician Certification Board (PTCB)/National Healthcare Association (NHA), required.
• NYSED- License
• Minimum of two (2) years experience as a Pharmacy Technician in a hospital pharmacy with a computerized system, preferred.
• Ability to learn computerized hospital pharmacy system.
Must be able to do physically strenuous work.
• Additional Salary Detail
The salary range and/or hourly rate listed is a good faith determination of potential base compensation that may be offered to a successful applicant for this position at the time of this job advertisement and may be modified in the future. When determining a team member's base salary and/or rate, several factors may be considered as applicable (e.g., location, specialty, service line, years of relevant experience, education, credentials, negotiated contracts, budget and internal equity).
The salary range for this position is $25-$25/hour
It is Northwell Health’s policy to provide equal employment opportunity and treat all applicants and employees equally regardless of their age, race, creed/religion, color, national origin, immigration status or citizenship status, sexual orientation, military or veteran status, sex/gender, gender identity, gender expression, disability, pregnancy, genetic information or genetic predisposition or carrier status, marital or familial status, partnership status, victim of domestic violence, sexual or other reproductive health decisions, or other characteristics protected by applicable law Show more details...
via Salary.com
schedule_type: Full-time
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description...
In-Vivo Technical Research Associate - Comparative Medicine
Are you looking
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description...
In-Vivo Technical Research Associate - Comparative Medicine
Are you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as an In-Vivo Technical Research Associate in our Cambridge office.
At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. As a Research Associate working on the Technical Services team within Comparative Medicine, you will be empowered to conduct in vivo studies and master technical skills.
POSITION OBJECTIVES:
• Provides in vivo technical support for studies supporting multiple therapeutic teams including Oncology, Neuroscience, GI and Vaccines. Includes work in BSL2 lab.
• Act as lead technician on studies and prepare study documentation.
• Manage sample transfers, formulation requests, and study updates with multiple groups.
• Manage integrity of data.
• Introduction to in vivo manipulations and techniques.
POSITION ACCOUNTABILITIES:
• Assist technical team in completing in vivo studies, gaining exposure to study design, technical procedures, and basic laboratory equipment
• Hands-on introduction to laboratory animal technical skills program
• Work in a team environment and collaborate on multiple tasks
• Record clear and concise study data with integrity
• Maintain study correspondence for assigned studies
• Track reporting deliverables and graph real-time data
EDUCATION, EXPERIENCE, BEHAVIOURAL COMPETENCIES AND SKILLS:
• Complete college level animal science/biology coursework
• Strong communication and organizational skills
• Proficiency with Microsoft Word, Microsoft Excel, and other common electronic systems
• Candidate should be able to work in a team environment to achieve objectives promptly
LICENSES/CERTIFICATIONS:
• AALAS Certification (not required, but preferred).
PHYSICAL DEMANDS:
• Ability to lift 50 lbs.
• Must be willing to work off-hours, holidays and weekends.
In accordance with the CO Equal Pay Act, Colorado Applicants Are Not Permitted to Apply
WHAT TAKEDA CAN OFFER YOU:
• 401(k) with company match and Annual Retirement Contribution Plan
• Tuition reimbursement
• Company match of charitable contributions
• Health & Wellness programs including onsite flu shots and health screenings
• Generous time off for vacation and the option to purchase additional vacation days
• Community Outreach Programs
Empowering Our People to Shine
Learn more at takedajobs.com.
No Phone Calls or Recruiters Please.
#LI-PW1
EEO Statement
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.
Locations
Cambridge, MA
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time Show more details...
Job Description...
In-Vivo Technical Research Associate - Comparative Medicine
Are you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as an In-Vivo Technical Research Associate in our Cambridge office.
At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. As a Research Associate working on the Technical Services team within Comparative Medicine, you will be empowered to conduct in vivo studies and master technical skills.
POSITION OBJECTIVES:
• Provides in vivo technical support for studies supporting multiple therapeutic teams including Oncology, Neuroscience, GI and Vaccines. Includes work in BSL2 lab.
• Act as lead technician on studies and prepare study documentation.
• Manage sample transfers, formulation requests, and study updates with multiple groups.
• Manage integrity of data.
• Introduction to in vivo manipulations and techniques.
POSITION ACCOUNTABILITIES:
• Assist technical team in completing in vivo studies, gaining exposure to study design, technical procedures, and basic laboratory equipment
• Hands-on introduction to laboratory animal technical skills program
• Work in a team environment and collaborate on multiple tasks
• Record clear and concise study data with integrity
• Maintain study correspondence for assigned studies
• Track reporting deliverables and graph real-time data
EDUCATION, EXPERIENCE, BEHAVIOURAL COMPETENCIES AND SKILLS:
• Complete college level animal science/biology coursework
• Strong communication and organizational skills
• Proficiency with Microsoft Word, Microsoft Excel, and other common electronic systems
• Candidate should be able to work in a team environment to achieve objectives promptly
LICENSES/CERTIFICATIONS:
• AALAS Certification (not required, but preferred).
PHYSICAL DEMANDS:
• Ability to lift 50 lbs.
• Must be willing to work off-hours, holidays and weekends.
In accordance with the CO Equal Pay Act, Colorado Applicants Are Not Permitted to Apply
WHAT TAKEDA CAN OFFER YOU:
• 401(k) with company match and Annual Retirement Contribution Plan
• Tuition reimbursement
• Company match of charitable contributions
• Health & Wellness programs including onsite flu shots and health screenings
• Generous time off for vacation and the option to purchase additional vacation days
• Community Outreach Programs
Empowering Our People to Shine
Learn more at takedajobs.com.
No Phone Calls or Recruiters Please.
#LI-PW1
EEO Statement
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.
Locations
Cambridge, MA
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time Show more details...
via Monster
posted_at: 8 days agoschedule_type: Full-time
Scientist (Vivo Immunology/Oncology)
Job Number: 23-00562
...
Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Scientist (Vivo Immunology/Oncology) for our client in Billerica, MA.
Eclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then
Scientist (Vivo Immunology/Oncology)
Job Number: 23-00562
...
Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Scientist (Vivo Immunology/Oncology) for our client in Billerica, MA.
Eclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!
Position Overview:
• Conducting in vivo pharmacology studies in murine tumor models
• Conducting PK/PD in vivo studies in murine models
Qualifications:
• Should be proficient in handling rodents (rats, and mice), able to prepare formulations, administer compounds via various routes (IV, PO, IP), and collect blood as well as various tissue samples for analysis.
• Also should be proficient in data collection/documentation in an electronic notebook format.
• Experience with the use of syngeneic or humanized models to study immunotherapies is highly desirable
• PhD in Immunology, Cell Biology, or other Science discipline or
• Master's degree in Immunology, Cell Biology, or other Science discipline with 3+ years' experience in Immunology and/or Immuno-Oncology (T Cell Biology) or Bachelor's degree in Immunology, Cell Biology, or other Science discipline with 5+ years' experience in Immunology and/or Immuno-Oncology (T Cell Biology)
If hired, you will enjoy the following Eclaro Benefits:
• 401k Retirement Savings Plan administered by Merrill Lynch
• Commuter Check Pretax Commuter Benefits
• Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro
If interested, you may contact:
Larah Beaniza
larah.robledo@eclaro.com
3322094549
Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status Show more details...
Job Number: 23-00562
...
Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Scientist (Vivo Immunology/Oncology) for our client in Billerica, MA.
Eclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!
Position Overview:
• Conducting in vivo pharmacology studies in murine tumor models
• Conducting PK/PD in vivo studies in murine models
Qualifications:
• Should be proficient in handling rodents (rats, and mice), able to prepare formulations, administer compounds via various routes (IV, PO, IP), and collect blood as well as various tissue samples for analysis.
• Also should be proficient in data collection/documentation in an electronic notebook format.
• Experience with the use of syngeneic or humanized models to study immunotherapies is highly desirable
• PhD in Immunology, Cell Biology, or other Science discipline or
• Master's degree in Immunology, Cell Biology, or other Science discipline with 3+ years' experience in Immunology and/or Immuno-Oncology (T Cell Biology) or Bachelor's degree in Immunology, Cell Biology, or other Science discipline with 5+ years' experience in Immunology and/or Immuno-Oncology (T Cell Biology)
If hired, you will enjoy the following Eclaro Benefits:
• 401k Retirement Savings Plan administered by Merrill Lynch
• Commuter Check Pretax Commuter Benefits
• Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro
If interested, you may contact:
Larah Beaniza
larah.robledo@eclaro.com
3322094549
Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status Show more details...
via LinkedIn
posted_at: 1 day agoschedule_type: Full-time
If you are a Associate Director, Non-clinical Development with extensive in-vivo experience, please read on!
We are a fast growing, late stage startup with exceptional funding looking to address one of the worlds biggest disease challenges, in an uncharted area of research. If you're looking for advanced, novel work, please apply to be considered and learn more...
Top Reasons to Work with Us
• High Job stability with $265m+ in funding
• Competitive
If you are a Associate Director, Non-clinical Development with extensive in-vivo experience, please read on!
We are a fast growing, late stage startup with exceptional funding looking to address one of the worlds biggest disease challenges, in an uncharted area of research. If you're looking for advanced, novel work, please apply to be considered and learn more...
Top Reasons to Work with Us
• High Job stability with $265m+ in funding
• Competitive compensation
• Opportunity for growth
• Mid-stage startup and still room to pave the way for the future of the company
• Exceptional benefits
• Convenient location in Cambridge
• Collaborative team and culture
What You Will Be Doing
• Participate in leading the Non-Clinical development team
• Help advance our functions (in pharmacology, non-clinical biology, in-vivo pharmacology and DMPK)
• Ensure delivery of the Non-Clinical IND work
• Be the spokesperson for our programs
• Meet deliverables on time
• Create and own a product development plan
Full JD available at sean.jenkins@cybercoders.com
What You Need for this Position
• PhD in Biology or similar
• 5-8+ years of biotech/pharma experience in industry
• Experience advancing R&D biologics programs
• Experience leading multi-disciplinary Non-Clinical Development Teams
• Expertise in Pharmacology, Non-Clinical Biology, DMPK/ and in vivo Pharmacology/Toxicology
• Previous experience leading successful scientific programs in in-vivo from discovery to IND
• Prior experience with a variety of animal models
So, if you are a Associate Director, Non-clinical Development (In-vivo) with experience, please apply today!
Colorado employees will receive paid sick leave. For additional information about available benefits, please contact Sean Jenkins
Email Your Resume In Word To
Looking forward to receiving your resume through our website and going over the position with you. Clicking apply is the best way to apply, but you may also:
Sean.Jenkins@CyberCoders.com
• Please do NOT change the email subject line in any way. You must keep the JobID: linkedin : SJ7-1720947 -- in the email subject line for your application to be considered.***
Sean Jenkins - Associate Manager - CyberCoders
Applicants must be authorized to work in the U.S.
CyberCoders, Inc is proud to be an Equal Opportunity Employer
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, or any other characteristic protected by law.
Your Right to Work – In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification document form upon hire Show more details...
We are a fast growing, late stage startup with exceptional funding looking to address one of the worlds biggest disease challenges, in an uncharted area of research. If you're looking for advanced, novel work, please apply to be considered and learn more...
Top Reasons to Work with Us
• High Job stability with $265m+ in funding
• Competitive compensation
• Opportunity for growth
• Mid-stage startup and still room to pave the way for the future of the company
• Exceptional benefits
• Convenient location in Cambridge
• Collaborative team and culture
What You Will Be Doing
• Participate in leading the Non-Clinical development team
• Help advance our functions (in pharmacology, non-clinical biology, in-vivo pharmacology and DMPK)
• Ensure delivery of the Non-Clinical IND work
• Be the spokesperson for our programs
• Meet deliverables on time
• Create and own a product development plan
Full JD available at sean.jenkins@cybercoders.com
What You Need for this Position
• PhD in Biology or similar
• 5-8+ years of biotech/pharma experience in industry
• Experience advancing R&D biologics programs
• Experience leading multi-disciplinary Non-Clinical Development Teams
• Expertise in Pharmacology, Non-Clinical Biology, DMPK/ and in vivo Pharmacology/Toxicology
• Previous experience leading successful scientific programs in in-vivo from discovery to IND
• Prior experience with a variety of animal models
So, if you are a Associate Director, Non-clinical Development (In-vivo) with experience, please apply today!
Colorado employees will receive paid sick leave. For additional information about available benefits, please contact Sean Jenkins
Email Your Resume In Word To
Looking forward to receiving your resume through our website and going over the position with you. Clicking apply is the best way to apply, but you may also:
Sean.Jenkins@CyberCoders.com
• Please do NOT change the email subject line in any way. You must keep the JobID: linkedin : SJ7-1720947 -- in the email subject line for your application to be considered.***
Sean Jenkins - Associate Manager - CyberCoders
Applicants must be authorized to work in the U.S.
CyberCoders, Inc is proud to be an Equal Opportunity Employer
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, or any other characteristic protected by law.
Your Right to Work – In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification document form upon hire Show more details...
via Careers Cannabis
schedule_type: Full-timesalary: 43K–220K a year
Job Description
Vivo HealthStaff is searching for Telemedicine Physicians licensed in Ohio for medical marijuana consultations...
Details :
• Work from home; Telecommute
• Choose your own schedule; Flexible hours.
• Provide medical marijuana consultations
Benefits :
• Competitive Rate
• Weekly payments via direct deposit
• Medical Malpractice provided
• Completely digital onboarding process
Requirements :
• Active medical
Job Description
Vivo HealthStaff is searching for Telemedicine Physicians licensed in Ohio for medical marijuana consultations...
Details :
• Work from home; Telecommute
• Choose your own schedule; Flexible hours.
• Provide medical marijuana consultations
Benefits :
• Competitive Rate
• Weekly payments via direct deposit
• Medical Malpractice provided
• Completely digital onboarding process
Requirements :
• Active medical license in Ohio
Last updated : 2022-04-22 Show more details...
Vivo HealthStaff is searching for Telemedicine Physicians licensed in Ohio for medical marijuana consultations...
Details :
• Work from home; Telecommute
• Choose your own schedule; Flexible hours.
• Provide medical marijuana consultations
Benefits :
• Competitive Rate
• Weekly payments via direct deposit
• Medical Malpractice provided
• Completely digital onboarding process
Requirements :
• Active medical license in Ohio
Last updated : 2022-04-22 Show more details...
via Salary.com
posted_at: 13 days agoschedule_type: Full-time
Qualifications Include:
• Architectural Degree with a focus on Interior Design preferred
• 5-10 years of experience working at a design firm...
• Solid knowledge of AutoCAD/Revit
• Exceptional graphic rendering skills,
preferably with Sketch-up and Adobe Suite
• Demonstrated high-quality design skills
• Ability to interpret a client’s program and develop space plans
• Selection and specification of interior finishes and furniture
•
Qualifications Include:
• Architectural Degree with a focus on Interior Design preferred
• 5-10 years of experience working at a design firm...
• Solid knowledge of AutoCAD/Revit
• Exceptional graphic rendering skills,
preferably with Sketch-up and Adobe Suite
• Demonstrated high-quality design skills
• Ability to interpret a client’s program and develop space plans
• Selection and specification of interior finishes and furniture
• Experience interfacing with clients, consultants, and contractors
• Ability to self-motivate and work independently when required
• Excellent verbal and written communication skills
Position Responsibilities Include:
• Interfacing with a Firm Principal
• Developing space plans and interior design concepts
• Preparing renderings and presentation materials
• Selecting materials, finishes, and furniture
• Contributing to the preparation of construction documents
and project deliverables.
Resumes should be sent to Matthew O'Brien at mobrien@vivoarch.co Show more details...
• Architectural Degree with a focus on Interior Design preferred
• 5-10 years of experience working at a design firm...
• Solid knowledge of AutoCAD/Revit
• Exceptional graphic rendering skills,
preferably with Sketch-up and Adobe Suite
• Demonstrated high-quality design skills
• Ability to interpret a client’s program and develop space plans
• Selection and specification of interior finishes and furniture
• Experience interfacing with clients, consultants, and contractors
• Ability to self-motivate and work independently when required
• Excellent verbal and written communication skills
Position Responsibilities Include:
• Interfacing with a Firm Principal
• Developing space plans and interior design concepts
• Preparing renderings and presentation materials
• Selecting materials, finishes, and furniture
• Contributing to the preparation of construction documents
and project deliverables.
Resumes should be sent to Matthew O'Brien at mobrien@vivoarch.co Show more details...
Norton safe Web