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CRN
CRN.com is a leading technology news and analysis website that covers the latest developments in the IT industry. It provides a wide range of news and articles on topics such as cloud computing, cybersecurity, data storage, networking, and software. The site offers a mix of original content and curated news from other sources to keep readers up-to-date with the latest technology trends. Besides, the site also features in-depth industry insights, interviews with experts, and product reviews. CRN.com is a go-to source for technology vendors, solution providers, and IT professionals looking for expert analysis, trending news, and insights into emerging technology markets.
Just prior to The Conference, CRN’s “day of science,” The Workshop, also drew an unprecedented number of participants.crnusa.orgAttendees heard from FDA Office of Dietary Supplements chief Steven Tave in addition to a diverse slate of business and marketing experts, political pundits, and of course, the CRN staff.
crn.comCRN editorial is the source Solution Providers turn to daily for breaking news, cutting-edge opinion by today's brightest Channel voices, and technical analysis by the acclaimed CRN Test Center.
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EncryptedSite is Encrypted
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CountryHosted in United States
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Latitude\Longitude37.751 / -97.822 Google Map
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Traffic rank#6,042 Site Rank
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Site age29 yrs old
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Site Owner informationWhois info
Website is Safe
Site is not blacklisted
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CategoriesTrade magazine
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PublisherThe Channel Company
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Founded1982
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First issueJune 7, 1982
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CompanyThe Channel Company
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CountryUnited States
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Based inWestborough, Massachusetts
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LanguageEnglish
Traffic rank
#6,042
#6,042
Site age
29 yrs
29 yrs
Location
United States
United States
Popular Questions for CRN
Newest job postings for CRN
via Glassdoor
posted_at: 10 days agoschedule_type: Full-time
This assertive, client-facing media architect will create, scope and present customized media and event proposals in a fast-paced, marketing environment. In this role, you will have deep understanding of today's ever-changing world of digital media and advertising and act as the expert in your field. Your campaign proposals will involve media and events strategies aimed at generating brand... awareness, driving website traffic and acquiring leads.
This assertive, client-facing media architect will create, scope and present customized media and event proposals in a fast-paced, marketing environment. In this role, you will have deep understanding of today's ever-changing world of digital media and advertising and act as the expert in your field. Your campaign proposals will involve media and events strategies aimed at generating brand... awareness, driving website traffic and acquiring leads. You will be helping multiple technology vendors increase awareness around their offerings and services within the IT channel to generate business.
Serving as a key resource, you'll routinely take center stage to create media and events campaign proposals that meet the objectives of your clients. You will architect, pitch, and close business, managing multiple campaign proposals simultaneously. To be successful in this role, you will be well-versed in the world of media, advertising and events, and will foster open and consistent communication with members of the Sales and Client Success Teams to deliver better-than-expected results.
This is an ideal situation for someone with a background in media and advertising and is looking to further their expertise in and around the IT channel.
Responsibilities:
• Ability to understand complex business and marketing issues and produce strategic marketing campaign proposals aimed at enhancing brand awareness, driving website traffic and growing partnerships.
• Manage all aspects of building proposals including collaboration with cross-functional teams inc. Sales and Sales Operations Teams, Client Success Managers and Reporting and Analytics Teams.
• Strong Analytical Skills- must possess the ability to understand traffic driving concepts, web technologies, website performance tracking and technology related issues in order to effectively propose programs, but also to guide teams through program improvements on a daily/weekly basis.
• Ability to understand business and marketing issues and how media and advertising are used to help clients overcome these issues.
• Drive strategic marketing discussions with internal stakeholders and present strategic proposals back to clients clearly and convincingly to secure business.
• Regularly communicate status of all proposed projects to internal and external team members.
• Draw upon quantitative and analytical skills to regularly monitor and make recommendations on how to optimize digital activities and capitalize on trends.
• Be the expert in media and advertising including technology, tools and strategies and stay current on new, emerging opportunities in the world of digital marketing.
Qualifications:
• Minimum 4yr degree in Advertising, Marketing, or related field with experience in the IT channel from either the vendor or solution provider side
• 4+ years of progressive Media and Ad industry experience
• Solid grasp of marketing tactics including in depth familiarity with awareness and demand generation activities to secure new business.
• Thrives in a fast-paced work environment and has demonstrated familiarity working in a high-throughput, high volume business.
• Must be skilled in Salesforce and Microsoft office suite (PowerPoint, Word, Excel) with interest in leaning new systems including web-based databases and analytics tools.
• Ability to work efficiently and independently while being part of a team and consistently displaying world-class professionalism at all times; attention to detail is a must.
• Strong interpersonal skills with an ability to articulate concepts and provide rationale to team members, stakeholders and clients on specific recommendations.
• Customer-service oriented; always friendly and approachable whether in person or via email and phone.
About The Channel Company:
Founded in 1982 and headquartered in Westborough, MA (30 miles west of Boston), TCC is the leading full-service channel enablement platform within the IT market, combining proprietary marketing, research, insights and data solutions with the industry’s most recognized editorial and media portfolio (CRN.com) and branded events including XChange, Midsize Enterprise Summit, Best of Breed and Woman of the Channel. With 150 employees across three offices in Massachusetts, New York and around the U.S., the Company maintains deep relationships with senior-level marketing and channel executives across every major technology company, providing best-in-class service in the increasingly complex IT channel.
Benefits:
All full-time employees of The Channel Company enjoy benefit offerings such as medical, dental, vision, tele-health, disability, life insurance, health savings accounts, paid parental leave, company matched 401k, unlimited PTO, sick time, and 15 company paid holidays. At The Channel Company we truly value work/life balance, are 100% remote, and employees enjoy flexible working hours. Beyond that, we are an innovative, collaborative, and inclusive group of employees who come together to overcome challenges and achieve best-in-class results.
• The Channel Company is licensed in the following states: AZ, CA, CT, DC, FL, GA, ID, IL, IN, KS, LA, MA, MD, ME, MI, MN, MO, MT, NC, NH, NJ, NV, NY, OR, PA, RI, TN, TX, UT, VA, WV. To be considered for this opportunity, you must reside in one of these listed states Show more details...
Serving as a key resource, you'll routinely take center stage to create media and events campaign proposals that meet the objectives of your clients. You will architect, pitch, and close business, managing multiple campaign proposals simultaneously. To be successful in this role, you will be well-versed in the world of media, advertising and events, and will foster open and consistent communication with members of the Sales and Client Success Teams to deliver better-than-expected results.
This is an ideal situation for someone with a background in media and advertising and is looking to further their expertise in and around the IT channel.
Responsibilities:
• Ability to understand complex business and marketing issues and produce strategic marketing campaign proposals aimed at enhancing brand awareness, driving website traffic and growing partnerships.
• Manage all aspects of building proposals including collaboration with cross-functional teams inc. Sales and Sales Operations Teams, Client Success Managers and Reporting and Analytics Teams.
• Strong Analytical Skills- must possess the ability to understand traffic driving concepts, web technologies, website performance tracking and technology related issues in order to effectively propose programs, but also to guide teams through program improvements on a daily/weekly basis.
• Ability to understand business and marketing issues and how media and advertising are used to help clients overcome these issues.
• Drive strategic marketing discussions with internal stakeholders and present strategic proposals back to clients clearly and convincingly to secure business.
• Regularly communicate status of all proposed projects to internal and external team members.
• Draw upon quantitative and analytical skills to regularly monitor and make recommendations on how to optimize digital activities and capitalize on trends.
• Be the expert in media and advertising including technology, tools and strategies and stay current on new, emerging opportunities in the world of digital marketing.
Qualifications:
• Minimum 4yr degree in Advertising, Marketing, or related field with experience in the IT channel from either the vendor or solution provider side
• 4+ years of progressive Media and Ad industry experience
• Solid grasp of marketing tactics including in depth familiarity with awareness and demand generation activities to secure new business.
• Thrives in a fast-paced work environment and has demonstrated familiarity working in a high-throughput, high volume business.
• Must be skilled in Salesforce and Microsoft office suite (PowerPoint, Word, Excel) with interest in leaning new systems including web-based databases and analytics tools.
• Ability to work efficiently and independently while being part of a team and consistently displaying world-class professionalism at all times; attention to detail is a must.
• Strong interpersonal skills with an ability to articulate concepts and provide rationale to team members, stakeholders and clients on specific recommendations.
• Customer-service oriented; always friendly and approachable whether in person or via email and phone.
About The Channel Company:
Founded in 1982 and headquartered in Westborough, MA (30 miles west of Boston), TCC is the leading full-service channel enablement platform within the IT market, combining proprietary marketing, research, insights and data solutions with the industry’s most recognized editorial and media portfolio (CRN.com) and branded events including XChange, Midsize Enterprise Summit, Best of Breed and Woman of the Channel. With 150 employees across three offices in Massachusetts, New York and around the U.S., the Company maintains deep relationships with senior-level marketing and channel executives across every major technology company, providing best-in-class service in the increasingly complex IT channel.
Benefits:
All full-time employees of The Channel Company enjoy benefit offerings such as medical, dental, vision, tele-health, disability, life insurance, health savings accounts, paid parental leave, company matched 401k, unlimited PTO, sick time, and 15 company paid holidays. At The Channel Company we truly value work/life balance, are 100% remote, and employees enjoy flexible working hours. Beyond that, we are an innovative, collaborative, and inclusive group of employees who come together to overcome challenges and achieve best-in-class results.
• The Channel Company is licensed in the following states: AZ, CA, CT, DC, FL, GA, ID, IL, IN, KS, LA, MA, MD, ME, MI, MN, MO, MT, NC, NH, NJ, NV, NY, OR, PA, RI, TN, TX, UT, VA, WV. To be considered for this opportunity, you must reside in one of these listed states Show more details...
via Women In Science
schedule_type: Full-time
About City of Hope
City of Hope is an independent biomedical research and treatment organization for cancer, diabetes and other life-threatening diseases...
Founded in 1913, City of Hope is a leader in bone marrow transplantation and immunotherapy such as CAR T cell therapy. City of Hope’s translational research and personalized treatment protocols advance care throughout the world. Human synthetic insulin, monoclonal antibodies and numerous breakthrough
About City of Hope
City of Hope is an independent biomedical research and treatment organization for cancer, diabetes and other life-threatening diseases...
Founded in 1913, City of Hope is a leader in bone marrow transplantation and immunotherapy such as CAR T cell therapy. City of Hope’s translational research and personalized treatment protocols advance care throughout the world. Human synthetic insulin, monoclonal antibodies and numerous breakthrough cancer drugs are based on technology developed at the institution. AccessHope™, a subsidiary launched in 2019 serves employers and their health care partners by providing access to City of Hope’s specialized cancer expertise.
A National Cancer Institute-designated comprehensive cancer center and a founding member of the National Comprehensive Cancer Network, City of Hope is ranked among the nation’s “Best Hospitals” in cancer by U.S. News & World Report and received Magnet Recognition from the American Nurses Credentialing Center. Its main campus is located near Los Angeles, with additional locations throughout Southern California and in Arizona.
City of Hope’s commitment to Diversity, Equity and Inclusion
We believe diversity, equity and inclusion is key in serving our mission to provide compassionate patient care, drive innovative discovery, and advance vital education focused on eliminating cancer and diabetes in all of our communities. Our commitment to Diversity, Equity and Inclusion ensures we bring the full range of skills, perspectives, cultural backgrounds and experiences to our work -- and that our teams align with the people we serve in order to build trust and understanding. We are dedicated to fostering a community that embraces diversity - in ideas, backgrounds and perspectives; this is reflected in our work and represented in our people.
Position Summary:
The Community Practice Clinical Research Nurse (CRN) is a Registered Nurse (RN) who works collaboratively with physicians, Clinical Research Site Schedulers (CRSSs), Clinical Research Coordinators (CRCs), Regulatory Coordinators (RCs) and pharmacists to coordinate care for an assigned population of patients who are enrolled onto IRB approved clinical research trials. The CRN assists in the assessment, management and coordination of outpatient care including triage of phone calls and proactive patient communication. The CRN serves to educate patients and families on the clinical trial treatments and required testing. The Clinical Research Nurse in collaboration with the CRC is responsible to ensure that the documentation for the clinical trial is complete and accurate.
Key Responsibilities include:
Management of Clinical Trials Patient
• Utilizes the City of Hope nursing process in clinical practice.
• Provides direct patient care for research related procedures for research patients, such as phlebotomy, including central lines, nursing assessments, and triage for research patients.
• Collaborates with the investigator to ascertain study patient eligibility for clinical trial, including documentation of criteria specified in the clinical trial.
• Assesses, identifies and prioritizes clinical information to physician, NP, PA and other clinicians for patients who are being evaluated or who are enrolled onto IRB clinical trials.
• Assesses and documents signs and symptoms of illness, reactions to treatment, changes in physical or psychological condition and general appearance in accordance with the IRB protocol assuring that the documentation is complete and accurate in order to avoid protocol deviations.
• Manage patient/family phone calls – collaborating with MD, NP and/or PA as needed to obtain orders for the management of the patient.
• Coordinates and communicates all aspects of care as defined by the protocol with the physician and other health care professionals and research team members.
• Collaborates with CRC to ensure that therapeutic clinical trial flag is activated in the patient’s EMR records during active treatment. Removes flag when patient is removed from clinical trial participation or when treatment is complete.
• Plans, coordinates and completes randomization (if applicable), patient assessments (toxicity assessment, diagnostic tests, and questionnaires), treatments and follow up care according to the defined protocol treatment plan.
• Collaborates with the physician and investigational pharmacists to ensure orders for treatment are written per protocol and delivered at the prescribed protocol intervals.
• Ensures that all documentation and required protocol documents are completed timely, completely and are legible.
• Collaborates with members of the interdisciplinary team to develop and implement the plan of care for the patient.
• Collects information from patient medical record, patient interviews, and diagnostic tests to determine eligibility of patient to be enrolled in the clinical trial. Communicates outcomes of eligibility to the physician.
• Supports and evaluates patient adherence to protocol and documents any deviations for adherence in the medical record.
• Collaborates as applicable with CRC for patients enrolled in clinical trials.
• Provides and documents education of patient and/or family regarding disease, treatment plan and follow up care.
• Administers (if applicable) and documents medications and evaluates the patient’s response to treatment. Ensures that the delivery of medication is safe and follows COH policies and procedures.
• Utilizes resources to learn about new medications or medications that are a part of an investigational research protocol.
• Participates in team meetings and other sponsor meetings as applicable.
Informed Consent Process
• Provide research patients with information associated with participation in a clinical research study: this includes both verbally and visually (paper or e-consent).
• Ensures the participant has adequate time to review the consent and ask questions.
• Responds to any inquiries about the study by the participant or family members.
• Alerts principal investigator of any concerns raised by the patient during the informed consent process.
• Ensure participant understands full the research project and able to freely give consent.
• Ensure all COH, federal and state regulations are followed for consenting non-English speaking patients or those whom cannot read, either English or their native language.
• Documents the consenting process in the electronic medical record (EMR).
• Conducts the consent process in compliance with any additional institutional, FDA, IRB, clinical trial sponsor and other applicable regulations.
• Ensures the consent process is performed and documented in compliance with institutional, FDA, IRB, clinical trial sponsor and other applicable regulations.
• Ensures that a copy of the signed consent is given to the patient and that it is scanned timely into the medical record.
• Ensures patients are appropriately scheduled, registered; maintains documentation of patient registration.
• Participates in the education of the patient regarding the clinical trial – documenting the education regarding the clinical trial in the medical record.
• Alerts principal investigator of any concerns raised by the patient during the informed consent process.
Protocol Compliance
• Demonstrates ability to multi-task, prioritize effectively and attention to detail to avoid protocol deviations.
• Assists internal or external study monitors in the protocol initiation and collaborates the review of documentation during protocol audits.
• Develops in collaboration with the investigational pharmacy and the principal investigator, study specific Beacon treatment plans for therapeutic clinical trials in EPIC. Ensures that the orders are reviewed, approved and published for use.
• Collaborates with principal investigators and Protocol Content Specialists (PCA) to ensure patient study calendars are created and accurately built within the clinical trials management system (OnCore).
• Promotes compliance with protocol procedures and processes as outlined in the clinical trial.
• Complies with the International Air Transport Association and institutional policies for shipping and receiving of biological specimens, experimental agents and devices.
• Provides education to nursing staff as applicable regarding the clinical trial to ensure that the protocol treatment plan is followed and that the medications are administered safely and as outlined in the clinical trial.
• Collaborates with scheduling staff to ensure that future appointments for the patients (follow up visits and diagnostic testing) are scheduled correctly and timely.
Other
• Participates in a collaborative, positive work environment as demonstrated through teamwork.
• Demonstrates a level of professional practice that supports the delivery of appropriate care and positive working relationship within the Modality team and through the medical center.
• Follows all COH policies and procedures when providing care. Provides care within the California nurse practice act. May provide direct clinical care to research patients.
• Delivers population specific care taking into consideration issues related to age, culture and other social issues.
• Ensures work environment is organized and functions efficiently. Participates in a collaborative, positive work environment as demonstrated through teamwork. Demonstrates a level of professional practice that supports the delivery of appropriate care and positive working relationship within the community practice research team and the clinical staff.
• Maintains current knowledge and awareness of organizational and regulatory standards, policies and procedures.
• Is self-motivated in organizing and follows through on assigned projects.
• Acts as a preceptor/mentor for new staff members and/or nursing students as applicable.
• Internal Contacts: Disease program lead physician, NP, PA, Clinical Pharmacist and other health care professionals who may be involved in the care of assigned patients.
• External Contacts: Outside MD, Pharmaceutical sponsor (if applicable), home care agencies and/or community resources as applicable.
• Practices a high level of integrity and honesty in maintaining confidentiality.
• Demonstrates a level of professional practice that supports the delivery of appropriate care and positive working relationship within the research team and throughout the medical center and medical foundation.
• Performs other related duties as assigned or requested.
Basic education, experience and skills required for consideration:
• BSN
• 2 or more years of experience in oncology and 2 or more yeas of experience in clinical trials research.
Or
• If prior clinical trial research is not oncology related, then a minimum of 4 years of non-oncology related clinical trials experience.
Required Certification/Licensure:
• ONS Chemotherapy/Biotherapy certification (can be completed within 1 year of hire date)
• Human Subjects Protection training (can be completed after hire)
• BLS from American Heart Association
• CA RN License
Additional Information:
As a condition of employment, City of Hope requires staff to comply with all state and federal vaccination mandates.
Salary / Pay Rate Information:
Pay Rate: $54.43 - $81.64 / hour
The estimated pay scale represents the typical [salary/hourly] range City of Hope reasonably expects to pay for this position, with offers determined based on several factors which may include, but not be limited to, the candidate’s experience, expertise, skills, education, job scope, training, internal equity, geography/market, etc. This pay scale is subject to change from time to time Show more details...
City of Hope is an independent biomedical research and treatment organization for cancer, diabetes and other life-threatening diseases...
Founded in 1913, City of Hope is a leader in bone marrow transplantation and immunotherapy such as CAR T cell therapy. City of Hope’s translational research and personalized treatment protocols advance care throughout the world. Human synthetic insulin, monoclonal antibodies and numerous breakthrough cancer drugs are based on technology developed at the institution. AccessHope™, a subsidiary launched in 2019 serves employers and their health care partners by providing access to City of Hope’s specialized cancer expertise.
A National Cancer Institute-designated comprehensive cancer center and a founding member of the National Comprehensive Cancer Network, City of Hope is ranked among the nation’s “Best Hospitals” in cancer by U.S. News & World Report and received Magnet Recognition from the American Nurses Credentialing Center. Its main campus is located near Los Angeles, with additional locations throughout Southern California and in Arizona.
City of Hope’s commitment to Diversity, Equity and Inclusion
We believe diversity, equity and inclusion is key in serving our mission to provide compassionate patient care, drive innovative discovery, and advance vital education focused on eliminating cancer and diabetes in all of our communities. Our commitment to Diversity, Equity and Inclusion ensures we bring the full range of skills, perspectives, cultural backgrounds and experiences to our work -- and that our teams align with the people we serve in order to build trust and understanding. We are dedicated to fostering a community that embraces diversity - in ideas, backgrounds and perspectives; this is reflected in our work and represented in our people.
Position Summary:
The Community Practice Clinical Research Nurse (CRN) is a Registered Nurse (RN) who works collaboratively with physicians, Clinical Research Site Schedulers (CRSSs), Clinical Research Coordinators (CRCs), Regulatory Coordinators (RCs) and pharmacists to coordinate care for an assigned population of patients who are enrolled onto IRB approved clinical research trials. The CRN assists in the assessment, management and coordination of outpatient care including triage of phone calls and proactive patient communication. The CRN serves to educate patients and families on the clinical trial treatments and required testing. The Clinical Research Nurse in collaboration with the CRC is responsible to ensure that the documentation for the clinical trial is complete and accurate.
Key Responsibilities include:
Management of Clinical Trials Patient
• Utilizes the City of Hope nursing process in clinical practice.
• Provides direct patient care for research related procedures for research patients, such as phlebotomy, including central lines, nursing assessments, and triage for research patients.
• Collaborates with the investigator to ascertain study patient eligibility for clinical trial, including documentation of criteria specified in the clinical trial.
• Assesses, identifies and prioritizes clinical information to physician, NP, PA and other clinicians for patients who are being evaluated or who are enrolled onto IRB clinical trials.
• Assesses and documents signs and symptoms of illness, reactions to treatment, changes in physical or psychological condition and general appearance in accordance with the IRB protocol assuring that the documentation is complete and accurate in order to avoid protocol deviations.
• Manage patient/family phone calls – collaborating with MD, NP and/or PA as needed to obtain orders for the management of the patient.
• Coordinates and communicates all aspects of care as defined by the protocol with the physician and other health care professionals and research team members.
• Collaborates with CRC to ensure that therapeutic clinical trial flag is activated in the patient’s EMR records during active treatment. Removes flag when patient is removed from clinical trial participation or when treatment is complete.
• Plans, coordinates and completes randomization (if applicable), patient assessments (toxicity assessment, diagnostic tests, and questionnaires), treatments and follow up care according to the defined protocol treatment plan.
• Collaborates with the physician and investigational pharmacists to ensure orders for treatment are written per protocol and delivered at the prescribed protocol intervals.
• Ensures that all documentation and required protocol documents are completed timely, completely and are legible.
• Collaborates with members of the interdisciplinary team to develop and implement the plan of care for the patient.
• Collects information from patient medical record, patient interviews, and diagnostic tests to determine eligibility of patient to be enrolled in the clinical trial. Communicates outcomes of eligibility to the physician.
• Supports and evaluates patient adherence to protocol and documents any deviations for adherence in the medical record.
• Collaborates as applicable with CRC for patients enrolled in clinical trials.
• Provides and documents education of patient and/or family regarding disease, treatment plan and follow up care.
• Administers (if applicable) and documents medications and evaluates the patient’s response to treatment. Ensures that the delivery of medication is safe and follows COH policies and procedures.
• Utilizes resources to learn about new medications or medications that are a part of an investigational research protocol.
• Participates in team meetings and other sponsor meetings as applicable.
Informed Consent Process
• Provide research patients with information associated with participation in a clinical research study: this includes both verbally and visually (paper or e-consent).
• Ensures the participant has adequate time to review the consent and ask questions.
• Responds to any inquiries about the study by the participant or family members.
• Alerts principal investigator of any concerns raised by the patient during the informed consent process.
• Ensure participant understands full the research project and able to freely give consent.
• Ensure all COH, federal and state regulations are followed for consenting non-English speaking patients or those whom cannot read, either English or their native language.
• Documents the consenting process in the electronic medical record (EMR).
• Conducts the consent process in compliance with any additional institutional, FDA, IRB, clinical trial sponsor and other applicable regulations.
• Ensures the consent process is performed and documented in compliance with institutional, FDA, IRB, clinical trial sponsor and other applicable regulations.
• Ensures that a copy of the signed consent is given to the patient and that it is scanned timely into the medical record.
• Ensures patients are appropriately scheduled, registered; maintains documentation of patient registration.
• Participates in the education of the patient regarding the clinical trial – documenting the education regarding the clinical trial in the medical record.
• Alerts principal investigator of any concerns raised by the patient during the informed consent process.
Protocol Compliance
• Demonstrates ability to multi-task, prioritize effectively and attention to detail to avoid protocol deviations.
• Assists internal or external study monitors in the protocol initiation and collaborates the review of documentation during protocol audits.
• Develops in collaboration with the investigational pharmacy and the principal investigator, study specific Beacon treatment plans for therapeutic clinical trials in EPIC. Ensures that the orders are reviewed, approved and published for use.
• Collaborates with principal investigators and Protocol Content Specialists (PCA) to ensure patient study calendars are created and accurately built within the clinical trials management system (OnCore).
• Promotes compliance with protocol procedures and processes as outlined in the clinical trial.
• Complies with the International Air Transport Association and institutional policies for shipping and receiving of biological specimens, experimental agents and devices.
• Provides education to nursing staff as applicable regarding the clinical trial to ensure that the protocol treatment plan is followed and that the medications are administered safely and as outlined in the clinical trial.
• Collaborates with scheduling staff to ensure that future appointments for the patients (follow up visits and diagnostic testing) are scheduled correctly and timely.
Other
• Participates in a collaborative, positive work environment as demonstrated through teamwork.
• Demonstrates a level of professional practice that supports the delivery of appropriate care and positive working relationship within the Modality team and through the medical center.
• Follows all COH policies and procedures when providing care. Provides care within the California nurse practice act. May provide direct clinical care to research patients.
• Delivers population specific care taking into consideration issues related to age, culture and other social issues.
• Ensures work environment is organized and functions efficiently. Participates in a collaborative, positive work environment as demonstrated through teamwork. Demonstrates a level of professional practice that supports the delivery of appropriate care and positive working relationship within the community practice research team and the clinical staff.
• Maintains current knowledge and awareness of organizational and regulatory standards, policies and procedures.
• Is self-motivated in organizing and follows through on assigned projects.
• Acts as a preceptor/mentor for new staff members and/or nursing students as applicable.
• Internal Contacts: Disease program lead physician, NP, PA, Clinical Pharmacist and other health care professionals who may be involved in the care of assigned patients.
• External Contacts: Outside MD, Pharmaceutical sponsor (if applicable), home care agencies and/or community resources as applicable.
• Practices a high level of integrity and honesty in maintaining confidentiality.
• Demonstrates a level of professional practice that supports the delivery of appropriate care and positive working relationship within the research team and throughout the medical center and medical foundation.
• Performs other related duties as assigned or requested.
Basic education, experience and skills required for consideration:
• BSN
• 2 or more years of experience in oncology and 2 or more yeas of experience in clinical trials research.
Or
• If prior clinical trial research is not oncology related, then a minimum of 4 years of non-oncology related clinical trials experience.
Required Certification/Licensure:
• ONS Chemotherapy/Biotherapy certification (can be completed within 1 year of hire date)
• Human Subjects Protection training (can be completed after hire)
• BLS from American Heart Association
• CA RN License
Additional Information:
As a condition of employment, City of Hope requires staff to comply with all state and federal vaccination mandates.
Salary / Pay Rate Information:
Pay Rate: $54.43 - $81.64 / hour
The estimated pay scale represents the typical [salary/hourly] range City of Hope reasonably expects to pay for this position, with offers determined based on several factors which may include, but not be limited to, the candidate’s experience, expertise, skills, education, job scope, training, internal equity, geography/market, etc. This pay scale is subject to change from time to time Show more details...
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