Clinical Research Coordinator

W2 Contract Role - 6-12 Months

Hybrid - Boston - On Site as needed (4 days per week likely on site)

Local W2 Candidates only - 1-2 Years of Expreience - $30-$35 / hr W2

• Work closely with research teams across the Department to ensure regulatory compliance and accurate data management collection
• The Regulatory Coordinator will work with investigators, staff, Institutional Review Boards (IRB), clinical trial sponsors and federal regulatory agencies to ensure that regulatory requirements for clinical trials are met for Clinical Trials.
• 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
• Maintenance of regulatory binders and other relevant files during the review, approval, and activation process for Clinical Trials

Qualifications