Clinical Trial Associate
Posted Updated
Description
JOB SUMMARY
The Clinical Trial Associate will be responsible supporting the clinical study team with administrative duties included but not limited to: collecting and reviewing essential regulatory documents, maintaining the trial master file and study status tracking.
RESPONSIBILITIES
- Timely and accurate review of essential regulatory documents (1572s, Informed Consents, Financial Disclosures, CVs) including communication of needed changes, as required, to PM, LCRA or site staff.
- Central IRB submission assistance.
- Tracking of study status.
- Maintenance of Clinical Trial Management System (CTMS).
- Creation, maintenance and archiving of trial master file (TMF).
- Shipment of study supplies.
- Meeting set-up and organization.
- Draft study meeting agendas/minutes.
- Liaise with Clinilabs’ clients as required per study.
- Site payment reconciliation assistance.
- Other study related administrative duties.
- Assist with training of new Clinical Trials Assistants.
- Participate in Clinical Operations departmental initiatives.
Salary range between $70,000 - $73,000. Final compensation is based on skills, experience, location, and overall expertise.
TRAVELING
From time to time, travel between company offices may be required, as needed.