Base: $24.28 - $39.43phly; bonus/equity: not speci...
Fully remote
2-3 years regulatory affairs experience
Bachelor's degree in healthcare or related field
Knowledge of good clinical practice guidelines
The position works independently under general supervision to ensure regulatory and operational requirements for clinical trials are met prior to activation
Job Summary
The position works independently under general supervision to ensure regulatory and operational requirements for clinical trials are met prior to activation.
This role involves maintaining electronic regulatory files, preparing protocol amendments, and submitting safety reports to the IRB and federal agencies.
Candidates must have a Bachelor's degree and 2-3 years of regulatory affairs experience with familiarity in GCP guidelines and relevant regulations.
Matching Summary
The position works independently under general supervision to ensure regulatory and operational requirements for clinical trials are met prior to activation.
Salary
Base: $24.28 - $39.43/Hourly; Bonus/Equity: Not specified; Benefits: Comprehensive benefits, career advancement opportunities, differentials, premiums, and bonuses
Skills & Requirements
Must-have
2-3 years regulatory affairs experience
Bachelor's degree in healthcare or related field
Knowledge of Good Clinical Practice guidelines
Nice-to-have
Ability to work independently and as a team member
Strong analytical and problem-solving skills
Excellent organizational and communication abilities
Key Requirements
Bachelor's Degree Healthcare Management or Related Field