
Regulatory Clinical Research Coordinator
- Boston, MA
- Permanent
- Full-time
-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
-Editing informed consent documents
-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 MonitorJOB REQUIREMENTSEDUCATION:
BA/BS requiredCERTIFICATES, LICENSES, REGISTRATIONS REQUIRED:
Human Subject Protections Certification, GCP CertificationEXPERIENCE:
Minimum of one year of experience in a research settingKNOWLEDGE AND SKILLS:
Excellent written and oral communication skills
Basic knowledge of and ability to operate various computer software applications, including but not limited to Outlook, Word, Excel, and Power Point.
Strong organizational, attentional to detail and multitasking skills