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via ICON Careers - ICON Plc
posted_at: 22 days agoschedule_type: Full-time
The team member will be responsible to read, comprehend, and translate clinical trial protocols /packaging specifications into clinical label generation software. individual will design clinical supplies trial labels for primary, secondary, and auxiliary packaging applications within the label systems. Individual will interpret randomization schemes, input into label software system, and utilize... system to verify correct labels are produced according
The team member will be responsible to read, comprehend, and translate clinical trial protocols /packaging specifications into clinical label generation software. individual will design clinical supplies trial labels for primary, secondary, and auxiliary packaging applications within the label systems. Individual will interpret randomization schemes, input into label software system, and utilize... system to verify correct labels are produced according to cGMPs.
Location: West Point, PA. Monday - Friday. 5 days weekly on-site.
Labeling, bottling and/or Translation of labels experience highly preferred.
Pharma/CRO experience highly preferred but other industry experience will be considered.
What you will be doing:
• Ensures all clinical supplies and associated documentation are processed according to GMPs/GDP’s and appropriate safety requirements to meet exacting standards defined by the team, the FDA and EU or other international regulatory agencies.
• May be responsible for any or all of the following:
• Coordination of Translation Requests
• Generation of Clinical Label Proofs with CLPG
• Liaise with country-level Clinical Operations personnel or Regulatory Affairs to address question, revise translations, update regulatory requirements, etc.
• Maintain Label Translations library
• Interpret clinical study design and Clinical Supply Strategy (CSS)
• Design and verify label models
• Coordinate MLBL manufacturing at vendor
• Perform visual inspection and accountability for label proofs, clinical labels and RCE’s
• Provide detailed analysis of issues and collaborate for creative problem solving
• Liaise with Clinical Supply Program Managers, Supply Planners, Quality, Pharmaceutical Sciences, or other stakeholders.
• May represent Clinical Packaging on internal or cross-functional teams. Will undertake and lead specific projects within the group on as needed basis
• Participate as necessary in complaint and deviation investigations with a focus on true root cause, and creation of
• appropriate Corrective and Preventative actions (CAPA's). Drive CAPA's to closure.
• Assist in training new team members and remain proficient in appropriate systems and software
• Responsible for the physical facility and good housekeeping practices within their area.
• Bachelor’s degree preferred Required Experience/Skills:
• 3+ years (with degree)
• 6+ years (without degree)
• Organization, detail oriented, equipment operation skills, equipment repair, problem solving, troubleshooting, interpersonal skills incl. verbal and written, multitasking, collaboration
• Able to connect the dots with task and identify future tasks to be done or whom to engage on next steps; understands supply chain and impact to success or failure of an action up and down the supply chain
Why ICON?
Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles Show more details...
Location: West Point, PA. Monday - Friday. 5 days weekly on-site.
Labeling, bottling and/or Translation of labels experience highly preferred.
Pharma/CRO experience highly preferred but other industry experience will be considered.
What you will be doing:
• Ensures all clinical supplies and associated documentation are processed according to GMPs/GDP’s and appropriate safety requirements to meet exacting standards defined by the team, the FDA and EU or other international regulatory agencies.
• May be responsible for any or all of the following:
• Coordination of Translation Requests
• Generation of Clinical Label Proofs with CLPG
• Liaise with country-level Clinical Operations personnel or Regulatory Affairs to address question, revise translations, update regulatory requirements, etc.
• Maintain Label Translations library
• Interpret clinical study design and Clinical Supply Strategy (CSS)
• Design and verify label models
• Coordinate MLBL manufacturing at vendor
• Perform visual inspection and accountability for label proofs, clinical labels and RCE’s
• Provide detailed analysis of issues and collaborate for creative problem solving
• Liaise with Clinical Supply Program Managers, Supply Planners, Quality, Pharmaceutical Sciences, or other stakeholders.
• May represent Clinical Packaging on internal or cross-functional teams. Will undertake and lead specific projects within the group on as needed basis
• Participate as necessary in complaint and deviation investigations with a focus on true root cause, and creation of
• appropriate Corrective and Preventative actions (CAPA's). Drive CAPA's to closure.
• Assist in training new team members and remain proficient in appropriate systems and software
• Responsible for the physical facility and good housekeeping practices within their area.
• Bachelor’s degree preferred Required Experience/Skills:
• 3+ years (with degree)
• 6+ years (without degree)
• Organization, detail oriented, equipment operation skills, equipment repair, problem solving, troubleshooting, interpersonal skills incl. verbal and written, multitasking, collaboration
• Able to connect the dots with task and identify future tasks to be done or whom to engage on next steps; understands supply chain and impact to success or failure of an action up and down the supply chain
Why ICON?
Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles Show more details...
via ZipRecruiter
posted_at: 1 day agoschedule_type: Full-timesalary: 45K–50K a year
Infinite Icons is seeking a vibrant, energetic, and dedicated entry-level Marketing Assistant to join our growing team! Our firm has been in the Washington DC area and was founded on the principles of excellent customer service and a dedication to providing our clients with the highest quality of marketing, sales, and advertising services. Our goal is to integrate creative marketing and sales... tactics in a new and innovative way with their consumer
Infinite Icons is seeking a vibrant, energetic, and dedicated entry-level Marketing Assistant to join our growing team! Our firm has been in the Washington DC area and was founded on the principles of excellent customer service and a dedication to providing our clients with the highest quality of marketing, sales, and advertising services. Our goal is to integrate creative marketing and sales... tactics in a new and innovative way with their consumer base to increase their brand awareness and long-term customer loyalty. Previously using this individualized approach with our entry-level Marketing Assistants saw profit margins increase, and the overall sales pipeline remained on a steady incline. This growth has led our company to search for a new member of our Marketing Team!
Our entry-level Marketing Assistant is someone integral to our success moving forward. They possess a student mentality with a friendly and inviting demeanor working with others. Our position is to start entry-level and provides one-on-one training in daily deliverables such as market/territory research, sales tactics, client communication, and reports directly to the Senior Marketing Manager.
Responsibilities & Core Deliverables of Our entry-level Marketing Assistant:
• Communicate and interact directly with clients and customers
• Conceptualize and lead promotional sales campaigns, working closely with the Senior Marketing Manager
• Identify specific target markets to help promote our clients’ products and services to
• Coordinate and present territory research to the rest of the entry-level and senior-level Marketing Team
• Develop and showcase leadership skills throughout the entry-level
• Build brand awareness and recognition through the implementation of individualized marketing and sales campaigns
• Support every angle of marketing with a customer-first approach to drive growth and brand loyalty
• Deliver results to our clientele daily and meet all objectives and goals
• Assist senior-level Marketing Manager with any other designated projects
Requirements & Expectations of Our entry-level Marketing Assistant:
• Associate’s degree or 4-year degree preferred
• 1 year of experience in customer service or customer-centric industry is required
• Ability to work in a fast-paced environment
• Highly motivated
• Team-oriented mindset
• Exceptional communication skills
• Versatile and dependable
• Friendly, positive, and upbeat personality
#LI-OnSite
Powered by JazzHR
CjRGJ9TYIj Show more details...
Our entry-level Marketing Assistant is someone integral to our success moving forward. They possess a student mentality with a friendly and inviting demeanor working with others. Our position is to start entry-level and provides one-on-one training in daily deliverables such as market/territory research, sales tactics, client communication, and reports directly to the Senior Marketing Manager.
Responsibilities & Core Deliverables of Our entry-level Marketing Assistant:
• Communicate and interact directly with clients and customers
• Conceptualize and lead promotional sales campaigns, working closely with the Senior Marketing Manager
• Identify specific target markets to help promote our clients’ products and services to
• Coordinate and present territory research to the rest of the entry-level and senior-level Marketing Team
• Develop and showcase leadership skills throughout the entry-level
• Build brand awareness and recognition through the implementation of individualized marketing and sales campaigns
• Support every angle of marketing with a customer-first approach to drive growth and brand loyalty
• Deliver results to our clientele daily and meet all objectives and goals
• Assist senior-level Marketing Manager with any other designated projects
Requirements & Expectations of Our entry-level Marketing Assistant:
• Associate’s degree or 4-year degree preferred
• 1 year of experience in customer service or customer-centric industry is required
• Ability to work in a fast-paced environment
• Highly motivated
• Team-oriented mindset
• Exceptional communication skills
• Versatile and dependable
• Friendly, positive, and upbeat personality
#LI-OnSite
Powered by JazzHR
CjRGJ9TYIj Show more details...
via Ladders
posted_at: 19 hours agoschedule_type: Full-timesalary: 101,014–151,522 a year
As a Global Clinical Trial Manager, you will play a key role in improving the lives of patients by accelerating the development of our customers ' drugs and devices through innovative solutions. You will be a dedicated resource to one of our clients, embedded in their working environment, systems, and processes.
What you will be doing...
• Primary point of contact to lead, manage and coordinate the conduct of clinical trials from study design to
As a Global Clinical Trial Manager, you will play a key role in improving the lives of patients by accelerating the development of our customers ' drugs and devices through innovative solutions. You will be a dedicated resource to one of our clients, embedded in their working environment, systems, and processes.
What you will be doing...
• Primary point of contact to lead, manage and coordinate the conduct of clinical trials from study design to close out at a global level in accordance with ICH-GCP, international regulations and sponsor SOPs
• Collaborate with Clinical Program Management teams for global execution of studies
• Ensure effective study risk management in place across all areas of studies
• Oversee and maintain the quality and scientific integrity of clinical operations for studies at a global level
• Collaborate with cross-functional internal and external stakeholders to ensure timely and on budget execution of clinical trial deliverables
• Proactively identify and communicate appropriately the status of ongoing studies, identified risks, mitigation strategies, associated action plans and issue resolution measures to ensure timely and on budget execution of study deliverables
You are:
• Education: BA/BS/BSc or RN
• Minimum of 4 years of clinical trial experience and 2 years of global clinical trial management experience.
• Broad experience working in life sciences or medically related field, including general biopharmaceutical clinical research experience (clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company).
• Excellent communication and interpersonal skills to effectively work with cross-functional teams.
• Knowledge of ICH/GCP and regulatory guidelines/directives.
#LI-Remote
Benefits of Working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That's why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know Show more details...
What you will be doing...
• Primary point of contact to lead, manage and coordinate the conduct of clinical trials from study design to close out at a global level in accordance with ICH-GCP, international regulations and sponsor SOPs
• Collaborate with Clinical Program Management teams for global execution of studies
• Ensure effective study risk management in place across all areas of studies
• Oversee and maintain the quality and scientific integrity of clinical operations for studies at a global level
• Collaborate with cross-functional internal and external stakeholders to ensure timely and on budget execution of clinical trial deliverables
• Proactively identify and communicate appropriately the status of ongoing studies, identified risks, mitigation strategies, associated action plans and issue resolution measures to ensure timely and on budget execution of study deliverables
You are:
• Education: BA/BS/BSc or RN
• Minimum of 4 years of clinical trial experience and 2 years of global clinical trial management experience.
• Broad experience working in life sciences or medically related field, including general biopharmaceutical clinical research experience (clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company).
• Excellent communication and interpersonal skills to effectively work with cross-functional teams.
• Knowledge of ICH/GCP and regulatory guidelines/directives.
#LI-Remote
Benefits of Working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That's why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know Show more details...
via ICON Careers - ICON Plc
schedule_type: Full-time
At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.
Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be... the Clinical Research Organisation that delivers
At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.
Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be... the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.
The Role:
•Collect all deliveries from loading bay, log, QC, receipt in, store and distribute as required.
• Maintain stock on shelves in a tidy manner, executing stock rotation in appropriate date order.
• Record all stock movements and stock issues using Inventory control system.
• Ensure accurate data entry.
• Operate all Inventory Control systems (e.g., IDBS, ASID, and Excel) and other appropriate systems to facilitate stock processing duties.
• Participate in stock cycle-counts.
• Liaise with internal customers, suppliers, and the Purchasing and Finance departments on all stock related issues.
• Perform any other duties as assigned by management
• Follow department SOPs.
• Other duties as assigned.
To be successful, you will need:
• C-High School or Equivalent (Required)
Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
Salary Range
$41,600 to $46,212
Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance.
Visit our careers site to read more about the benefits ICON offers Show more details...
Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be... the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.
The Role:
•Collect all deliveries from loading bay, log, QC, receipt in, store and distribute as required.
• Maintain stock on shelves in a tidy manner, executing stock rotation in appropriate date order.
• Record all stock movements and stock issues using Inventory control system.
• Ensure accurate data entry.
• Operate all Inventory Control systems (e.g., IDBS, ASID, and Excel) and other appropriate systems to facilitate stock processing duties.
• Participate in stock cycle-counts.
• Liaise with internal customers, suppliers, and the Purchasing and Finance departments on all stock related issues.
• Perform any other duties as assigned by management
• Follow department SOPs.
• Other duties as assigned.
To be successful, you will need:
• C-High School or Equivalent (Required)
Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
Salary Range
$41,600 to $46,212
Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance.
Visit our careers site to read more about the benefits ICON offers Show more details...
via Built In
posted_at: 11 days agoschedule_type: Full-time
At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.
Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence
At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.
Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That's our vision. We're driven by it. And we need talented people who share it.
If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.
The Role:
As a member of the Study Start Up Team, you will play an integral role in making sure that physicians at our research sites... are prepared to start the trial of investigational, new pharmaceutical and biological products for clinical trials at their local practices.• Coordinate, balance and facilitate activities related to the completion of Critical Document Package (CDP) and the IP release checklist (SST004-SOP-F01) in accordance with ICH GCP guidelines and all applicable regulations, laws, ethical standards, other guidelines, sponsor requirements• Ensure that the overall process is focused on quality, efficiency and cost containment for a particular region / sub division within the CDP group, under the general mentorship of Mgr/Sr. Manager - Central Services or Designee.
Your Profile• A high school diploma or local equivalent• Bachelor's Degree Required (preferably in Life Sciences)• Minimum of 1 years' experience or understanding of clinical study start up requirements and activities.• Experience of Clinical Trial operations and meeting regulatory guidelines• Proficient project management skills.
Office with Flex position: 60% in office and 40% Remote
Office options: Raleigh, NC, Wilmington, NC, Blue Bell, PA, Lenexa KS and Nashville, TN
Benefits of Working in ICON:
Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
#LI-TG2
#LI-HYBRID
Are you a current ICON Employee? Please click here to apply: link Show more details...
Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That's our vision. We're driven by it. And we need talented people who share it.
If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.
The Role:
As a member of the Study Start Up Team, you will play an integral role in making sure that physicians at our research sites... are prepared to start the trial of investigational, new pharmaceutical and biological products for clinical trials at their local practices.• Coordinate, balance and facilitate activities related to the completion of Critical Document Package (CDP) and the IP release checklist (SST004-SOP-F01) in accordance with ICH GCP guidelines and all applicable regulations, laws, ethical standards, other guidelines, sponsor requirements• Ensure that the overall process is focused on quality, efficiency and cost containment for a particular region / sub division within the CDP group, under the general mentorship of Mgr/Sr. Manager - Central Services or Designee.
Your Profile• A high school diploma or local equivalent• Bachelor's Degree Required (preferably in Life Sciences)• Minimum of 1 years' experience or understanding of clinical study start up requirements and activities.• Experience of Clinical Trial operations and meeting regulatory guidelines• Proficient project management skills.
Office with Flex position: 60% in office and 40% Remote
Office options: Raleigh, NC, Wilmington, NC, Blue Bell, PA, Lenexa KS and Nashville, TN
Benefits of Working in ICON:
Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
#LI-TG2
#LI-HYBRID
Are you a current ICON Employee? Please click here to apply: link Show more details...
via Built In
posted_at: 24 days agoschedule_type: Full-time
At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.
Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organization: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organization that delivers excellence
At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.
Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organization: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organization that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That's our vision. We're driven by it. And we need talented people who share it.
If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.
Title: Clinical Research Coordinator 2 (CRC 2)
Location: On-Site, McFarland IA
Summary: The CRC 2 ensures the safety of our... participants, promotes the mission of Accellacare, and consistently strides to meet and exceed priorities discussed with supervisor. The CRC 2 will actively recruit and promote our service to suitable participants and sponsor representatives. Additionally, the CRC 2 will autonomously perform tasks required to coordinate and complete multiple studies according to the protocol. Lastly, they will assist the Manager of Clinical Operations and Sr. Clinical Research Coordinators with staff development through mentoring and site level quality assurance.
Duties: • Performs study start-up duties including the production of a recruitment tool, and progress notes, as well as phone screening patients and identifying participants for trials on site• Proactively develops and executes recruitment plans that meet and exceed enrollment goals• Performs study start-up duties including the production of a recruitment plan, recruitment tool, and progress notes, as well as phone screening participants.• Completes training on Clinical Trial Management System and maintains proper skills to update database, complete participant reimbursement, capture referral source of participants, and create calls lists to promote recruitment. • Attends investigator meetings • Creates and updates source documents/progress notes and utilizes templates provided in the Core Operating Guidelines• Accurately collects study data via source documents/progress notes as required by the protocol• Performs technical requirements of the study protocol, i.e., lab work (phlebotomy and processing), blood pressure, electrocardiograms, Holtor monitoring, pulmonary function testing, allergy testing, urine/serum pregnancy testing, strep throat screening, or any procedure necessary for the protocol as ordered by the investigator or specified by a protocol• Performs continuous reviews of the inclusion and exclusion criteria for each participant during the trial for their trials as well as peer review of inclusion and exclusion for trials• Documents laboratory data and adverse reactions, presents this information to an investigator in a timely manner, and immediately notifies investigators, the Institutional Review Board and sponsor of any serious adverse events • Builds and maintains strong relationships with Investigators and provides ongoing communication about trial status and participants • Dispenses study medication at the direction of the Investigator• Maintains communication with the monitor from the sponsoring company through telephone contact, written communication and on-site visits• Enters visit data in the Electronic Data Capture (EDC) or Case Report Forms (CRF) within timelines provided by sponsor
To be successful, you will have:
• Bachelor's Degree
• 2 + years of experience as a clinical research coordinator or equivalent role
• High attention to detail
Benefits of Working in ICON:
Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
Are you a current ICON Employee? Please click here to apply: link Show more details...
Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organization: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organization that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That's our vision. We're driven by it. And we need talented people who share it.
If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.
Title: Clinical Research Coordinator 2 (CRC 2)
Location: On-Site, McFarland IA
Summary: The CRC 2 ensures the safety of our... participants, promotes the mission of Accellacare, and consistently strides to meet and exceed priorities discussed with supervisor. The CRC 2 will actively recruit and promote our service to suitable participants and sponsor representatives. Additionally, the CRC 2 will autonomously perform tasks required to coordinate and complete multiple studies according to the protocol. Lastly, they will assist the Manager of Clinical Operations and Sr. Clinical Research Coordinators with staff development through mentoring and site level quality assurance.
Duties: • Performs study start-up duties including the production of a recruitment tool, and progress notes, as well as phone screening patients and identifying participants for trials on site• Proactively develops and executes recruitment plans that meet and exceed enrollment goals• Performs study start-up duties including the production of a recruitment plan, recruitment tool, and progress notes, as well as phone screening participants.• Completes training on Clinical Trial Management System and maintains proper skills to update database, complete participant reimbursement, capture referral source of participants, and create calls lists to promote recruitment. • Attends investigator meetings • Creates and updates source documents/progress notes and utilizes templates provided in the Core Operating Guidelines• Accurately collects study data via source documents/progress notes as required by the protocol• Performs technical requirements of the study protocol, i.e., lab work (phlebotomy and processing), blood pressure, electrocardiograms, Holtor monitoring, pulmonary function testing, allergy testing, urine/serum pregnancy testing, strep throat screening, or any procedure necessary for the protocol as ordered by the investigator or specified by a protocol• Performs continuous reviews of the inclusion and exclusion criteria for each participant during the trial for their trials as well as peer review of inclusion and exclusion for trials• Documents laboratory data and adverse reactions, presents this information to an investigator in a timely manner, and immediately notifies investigators, the Institutional Review Board and sponsor of any serious adverse events • Builds and maintains strong relationships with Investigators and provides ongoing communication about trial status and participants • Dispenses study medication at the direction of the Investigator• Maintains communication with the monitor from the sponsoring company through telephone contact, written communication and on-site visits• Enters visit data in the Electronic Data Capture (EDC) or Case Report Forms (CRF) within timelines provided by sponsor
To be successful, you will have:
• Bachelor's Degree
• 2 + years of experience as a clinical research coordinator or equivalent role
• High attention to detail
Benefits of Working in ICON:
Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
Are you a current ICON Employee? Please click here to apply: link Show more details...
via Glassdoor
schedule_type: Full-timesalary: 22–31 an hour
PRN Shifts
We are looking for RN's and/or LVN's to provide in home nursing care to one of our pediatric patients in Conroe, Texas. This is patient has 84 hours weekly. The preferred schedule during School is Monday - Friday 3p-11p and Saturday/Sunday 10a-10:30p. Weekend hours do offer some flexibility...
This is a sweet 18-year-old female that requires GB feeds and diaper changes.
Pay is based on if you are an LVN or an RN.
We are looking for
PRN Shifts
We are looking for RN's and/or LVN's to provide in home nursing care to one of our pediatric patients in Conroe, Texas. This is patient has 84 hours weekly. The preferred schedule during School is Monday - Friday 3p-11p and Saturday/Sunday 10a-10:30p. Weekend hours do offer some flexibility...
This is a sweet 18-year-old female that requires GB feeds and diaper changes.
Pay is based on if you are an LVN or an RN.
We are looking for immediate hire!
If you have questions, or would like to schedule an interview, please contact our office at 832-930-9500 or submit your resume and someone will reach out to you soon.
Job Type: Full-time
Pay: $22.00 - $31.00 per hour
Medical specialties:
• Home Health
• Pediatrics
Standard shift:
• Day shift
• Evening shift
Weekly schedule:
• Every weekend
• Monday to Friday
• Rotating weekends
• Weekends as needed
License/Certification:
• BLS Certification (Preferred)
• RN License and LVN License (Required)
Work Location: Multiple locations Show more details...
We are looking for RN's and/or LVN's to provide in home nursing care to one of our pediatric patients in Conroe, Texas. This is patient has 84 hours weekly. The preferred schedule during School is Monday - Friday 3p-11p and Saturday/Sunday 10a-10:30p. Weekend hours do offer some flexibility...
This is a sweet 18-year-old female that requires GB feeds and diaper changes.
Pay is based on if you are an LVN or an RN.
We are looking for immediate hire!
If you have questions, or would like to schedule an interview, please contact our office at 832-930-9500 or submit your resume and someone will reach out to you soon.
Job Type: Full-time
Pay: $22.00 - $31.00 per hour
Medical specialties:
• Home Health
• Pediatrics
Standard shift:
• Day shift
• Evening shift
Weekly schedule:
• Every weekend
• Monday to Friday
• Rotating weekends
• Weekends as needed
License/Certification:
• BLS Certification (Preferred)
• RN License and LVN License (Required)
Work Location: Multiple locations Show more details...
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