Clinical Trial Coordinator (Sponsor Dedicated/ US Remote)
$47,000–$79,900 year
RemoteUnited States
Job Summary
Maintain and close out project files, including regulatory documents, Trial Master Files, enrollment data, and adverse events, across various databases. Distribute study-specific financial reports, prepare and circulate meeting minutes with action items, and track Key Performance Indicators with oversight from the Project Lead. Provide status updates to customers, ensure document archiving per guidelines, and support quality assurance activities by preparing for audits and resolving actionable issues. May serve as the primary customer contact, mentor Project Specialists, and lead internal or external meetings as directed. Operates independently with minimal oversight to ensure contracted services meet customer requirements.
Required Qualifications
- Moderate relevant clinical research experience
- Understanding of clinical drug development
- Understanding of clinical trial operations
- Strong knowledge of Good Clinical Practice/ICH guidelines
- Knowledge of other applicable regulatory requirements
- High proficiency with Veeva Applications
- High proficiency with full MS Office Applications
- Strong communication, presentation, interpersonal skills, both written and spoken
- Ability to inform, influence, convince, and persuade
- High level of competence in English language
Desired Qualifications
- Prefer candidates with some combination of education and experience in life sciences, Medicine, Pharmacy, Nursing or related field
- Experience in a therapeutic group preferred
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