Search Results: 8,849 vacancies
...Job Description
The Sr. IRB Analyst provides administrative and regulatory support for the IRB staff, the IRB Chairs, the IRB Board members and the institution's researchers. The Sr. IRB Analyst processes IRB submissions, serves as an alternate voting member on the...
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For contractors
...Day (United States of America)
Job Summary: The Regulatory Coordinator performs all basic regulatory administrative tasks and submissions... .... Responds clearly & promptly to questions & comments from IRB and/or sponsor. Completes application forms accurately & with attention...
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Work experience placement
Immediate start
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...Clinical Research Coordinator
Department: Operations
Employment Type: Full Time
Location: Boston Clinical Trials | Roslindale... ...timely manner;
o Filing SAE/Deviation reports to Sponsor and IRB as needed;
o Documenting and reporting adverse events;
o...
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Full time
Temporary work
...seek an organized, highly motivated, full-time Clinical Research Coordinator I (CRC) to join our Dystonia Partners Research Bank team in the... ...research study(s).
* Assists with regulatory binders, IRB protocol submission, and quality assurance/quality improvement...
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Full time
Bank staff
Remote job
...can be accommodated.
Job Overview:
The Clinical Research Coordinator, Level 1 (CRC1) is a research professional who ensures... ...including all study, investigator and Institutional Review Board (IRB) information, and patient
recruitment activity
* Actively...
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Local area
...and the Support Services Core.
The DCR Sr. Clinical Research Coordinator provides support and oversight of clinical research projects... ...according to the ICH Good Clinical Practice (ICH GCP) guidelines, FDA, IRB, and applicable state and local regulations. Supports the DCR...
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Work experience placement
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...Lead, the Senior Research Assistant will be responsible for the coordination of clinical research trial(s) related to Aging and Metabolism.... ...of data and study documentation for Institutional Review Board (IRB), clinical research forms, and quality assurance. Some studies...
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...GENERAL SUMMARY/ OVERVIEW STATEMENT:
Will be responsible for coordinating referrals and desensitizations at four different locations... ...projects is preferred but not required. Excellent knowledge of IRB regulations regarding human subjects and clinical research is preferred...
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Traineeship
...Job Summary
The IRB Administrator is part of a team that reviews and approves human subjects research protocols overseen by the Harvard University-Area (HUA) IRB. The IRB Administrator:
Collaborates with researchers, the IRB Chairperson and IRB members, and other...
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Remote job
...be responsible for supporting all aspects of clinical research coordination for studies at the NCRI. The research trials may include treatment... ...forms.
* Corresponds with the Institutional Review Board (IRB) for approval of protocol, notification of adverse events, continuation...
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Rotating shift
...highly motivated individuals that come together to form high performance team? Come join WWT today! We are looking for a Project Coordinator to join our Infrastructure Services (IS).
Why should you join the PMO?
As a Project Coordinator, you will be working on exciting...
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Full time
Contract work
...scheduling tests and arranging admissions or outpatient visits for patients. (essential)
8. Assists investigator with correspondence with IRB. (essential)
Required Qualifications:
~ Bachelor's degree required; Master's degree preferred.
~1-3 years related work...
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Immediate start
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...A reputable hospital in Boston is looking for a Care Coordinator to join their team.
The Care Coordinator (Manager) is responsible for managing care insurance referral requests for patients of Primary Care Practices and emphasizing patient-centered care, timeliness...
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...a member of the clinical research team, the Clinical Research Coordinator II contributes to the conduct of a portfolio of clinical research... ...and other safety reports to the Institutional Review Board (IRB), sponsors, and other entities, as warranted and according to required...
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Contract work
Flexible hours
...Client Service Coordinator
West Somerville, MA (onsite)
Overview:
We are currently hiring an Ambulatory Administrative Support Specialist to provide essential administrative assistance in our healthcare center. This role involves managing patient interactions...
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Currently hiring
...providing support to clinical research studies. Independently coordinates all activities of clinical trials and clinical research including... ..., data collection systems, and institutional review board (IRB) approval.
13. Assorted administrative work on participant and...
We are hiring a Clinical Research Coordinator I to be involved in studies of human brain structure and function using state-of-the-art imaging... ...assurance and accuracy
* Ensure compliance of study with IRB and other regulations,
* Prepare amendments and annual progress...
Part time
...research interviews, focus groups and email communications 3. Participates in development and submission of study related documents to the IRB for each assigned study(s) 4. Participates in data analysis, programming, data management, abstracts, data tables, and presentations...
Work experience placement
Immediate start
Shift work
...oversight for review operations of the Harvard University Area (HUA) IRB, including the management and supervision of IRB review staff.... ..., HUA researchers, and participant outreach including the coordination of continuing education and development of professional development...
...We seek a highly proficient Spanish-speaking Clinical Research Coordinator (CRC) to join the MGH Early Brain Development Initiative, a collaboration... ...and focus groups
* Ensure compliance with federal and IRB regulations
* Assist with IRB submissions, amendments and...
Work experience placement
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