FSP Clinical Trial Coordinator

Job Title: FSP Clinical Trial Coordinator Job Location: Remote, North Carolina, USA Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our global team, you’ll have the opportunity to provide administrative and technical support to the Project Team. As a Clinical Trial Coord, you'll support audit readiness by ensuring files are reviewed according to the schedule detailed in the organization's SOP and department guidance document.

You will provide administrative support for site activation activities and aid in the development of the critical path for site activation within assigned projects to support rapid site activations.

Representing CRG personnel, you may utilize local knowledge, organization systems, external site lists, and sponsor directives to develop and review site lists that are suitable for the strategic needs of feasibility activities and to provide local input into the site tiering process.

Additionally, you may act as a buddy during the onboarding phase and provide training to new staff as needed. What You’ll Do: According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trial(s) activities as detailed on the task matrix.

•Performs department, Internal, Country and Investigator file reviews as assigned, and documents findings in appropriate system(s).

•Ensures allocated tasks are performed on time, within budget and to a high-quality standard. Proactively communicates any risks to project leads.

•Provides system support (i.e., Activate & eTMF) and ensures system databases are always current.

•Performs administrative tasks on assigned t