Clinical Trial Coordinator
2 months ago
About the Role:
The Clinical Trial Assistant will play a crucial role in the day-to-day management of clinical trials at investigative sites. This position requires a detail-oriented individual with excellent organizational skills to ensure the smooth execution of clinical trials.
Key Responsibilities:
- Review and track progress of clinical trials, ensuring compliance with regulatory requirements and standard operating procedures.
- Collect and file essential regulatory documentation from clinical sites, including financial disclosures, debarment checks, and current CVs.
- Support the development of case report forms and case report form completion guidelines.
- Assist with user acceptance testing of eTMF and databases.
- Coordinate archiving of study relevant documents/files and ensure audit and inspection readiness.
- Provide updates to study specific internal data repositories to ensure availability of trial documents to the study team.
Requirements:
- BA/BS degree in Life Sciences, Nursing, or related scientific field (or equivalent experience).
- 1-2 years of relevant clinical trial experience with associated skill sets.
- Previous experience in the pharmaceutical industry/biotech is desirable.
What We Offer:
Bolt Medical is a dynamic and innovative company that values its employees. As a Clinical Trial Assistant, you will have the opportunity to work in a fast-paced environment with a team of experienced professionals. We offer a competitive salary and benefits package, as well as opportunities for professional growth and development.
Location:
Hybrid: Onsite- Carlsbad, California Office at least 3 days per week.
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