Clinical Research Coordinator

Core duties include:

Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out.

*Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies.

*Coordinate the collection of study specimens and processing.

*Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets and other study-related documents, and complete study documents/case report forms.

*Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions and ensure Institutional Review Board renewals are completed.

*Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.

*Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff.

*Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.

*Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.

*Participate in monitoring visits and regulatory audits.

Job Type: Contract

Pay: $40.00 - $48.00 per hour

Expected hours: 40 per week

Work Location: In person