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Clinical Research Coordinator
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Boston, Massachusetts, United States Alcanza Clinical Research Full time $60,000 - $90,000 per yearClinical Research CoordinatorDepartment: Operations Employment Type: Full TimeLocation: Boston Clinical Trials | Roslindale, MAReporting To: Joanne MonaghanDescription Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in MA, NH, MI, VA, SC, FL, GA, AL, MO, TX and Puerto Rico. We have established a strong...
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Clinical Research Coordinator
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Boston, United States Alcanza Clinical Research Full timeClinical Research CoordinatorAlcanza is a growing multi-site, multi-phase clinical research company with a network of locations in MA, NH, MI, VA, SC, FL, GA, AL, MO, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine....
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Clinical Research Site Director
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Clinical Research Associate
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Clinical Research Coordinator
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Boston, United States Massachusetts General Hospital Full timeClinical Research Coordinator-(3294569) Description GENERAL SUMMARY/ OVERVIEW STATEMENT : PRINCIPAL DUTIES AND RESPONSIBILITIES : The CRC I will work closely with investigators, post-docs, and study staff to oversee current and upcoming studies. The CRC I’s responsibilities may include but are not limited to: Conduct TMS, tDCS, MRI and EEG experiments....
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Clinical Research Coordinator
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Clinical Research Coordinators
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Boston, United States Advarra, Inc. Full timeAt Advarra, we seek to foster an inclusive and collaborative environment where everyone is treated with respect and diverse perspectives are embraced. Treating one another, our clients and clinical trial participants with empathy and care are key tenets of our culture at Advarra; we are committed to creating a workplace where each person is not only valued...
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Clinical Research Coordinator
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Boston, United States Massachusetts General Hospital Full timeThe Cancer Center Protocol Office is seeking motivated, detail-oriented individuals to join our team as a Clinical Research Coordinator. The Cancer Center Protocol Office is a centralized clinical research office that supports clinical researchers in all disciplines within the Cancer Center. Our office promotes and facilitates clinical research by providing...
Clinical Research Coordinator
4 weeks ago
Overview POSITION SUMMARY: As a direct report to the Clinical Research Director, the Regulatory Coordinator works closely with research teams across the Department to ensure regulatory compliance and accurate data management collection for multiple cancer trials. The Regulatory Coordinator will work with investigators, study staff, Institutional Review Boards (IRB), clinical trial sponsors and federal regulatory agencies to ensure that regulatory requirements for clinical trials are met. This position does not involve patient contact, but may include data abstraction from patient records. Responsibilities Schedule and facilitate pre-activation activities including pre-site qualification visits, SIVs, and facility tours Complete feasibility questionnaires for upcoming studies Assist in start-up and implementation activities for new studies Completion and submission of clinical trials amendments to the IRB Correspondence with the IRB, investigators and sponsors throughout the clinical trial process Prepares annual progress reports for IRB renewal of ongoing studies Collection, completion, and submission of regulatory documents to various regulatory entities Maintenance of regulatory binders and other relevant files during the review, approval, and activation process for Clinical Trials Coordinates Review & Processing of Safety Reports to the IRB Manages data collection via chart abstraction and submits data in timely fashion Manages and possibly reports Adverse Events & Deviations reported to the IRB and Sponsors Resolves data discrepancies as requested by Sponsors Participates in monitoring visits as requested by Sponsors and makes data corrections as required by Monitor Qualifications EDUCATION: BA/BS required CERTIFICATES, LICENSES, REGISTRATIONS REQUIRED: Human Subject Protections Certification, GCP Certification EXPERIENCE: Minimum of one year of experience in a research setting Seniority level Associate Employment type Contract Job function Other Industries Pharmaceutical Manufacturing Biotechnology Research Research Services #J-18808-Ljbffr
