Senior Clinical Trial Associate
Job Summary
Supporting the implementation and conduct of clinical studies, the full-time Senior Clinical Trial Associate will collaborate with clinical operations teams to ensure compliance with regulatory requirements and assist in various clinical trial tasks in a remote setting.
Key responsibilities
- Collaborates with CTM/Sr. CTM on clinical planning, protocol development, and site selection for clinical trials
- Ensures compliance with FDA regulations and company SOPs during clinical investigations and post-market studies
- Tracks study-specific payments and assists in administrative documentation related to clinical study programs
Required qualifications
- Bachelor's degree in a health profession or science; advanced degree preferred
- At least 3 years of ongoing clinical trials experience
- Proficiency in GCPs and knowledge of FDA regulatory requirements
- Familiarity with medical terminology
- Ability to work independently and effectively
Complete Job Description
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