Clinical Trial Associate III
Behavioral Health Market Context
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Job Description
ired Qualifications
Bachelor's degree or international equivalent in a clinical, biological, scientific, or health-related field
5+ years of practical experience in clinical trial administration (e.g., Inhouse CRA, CTA, site administration)
Strong knowledge of clinical studies and TMF functionality in accordance with study-specific plans and SOPs
Ability to work independently and manage multiple projects in a fast-paced environment
Preferred location: East Coast
Bachelor's degree or international equivalent in a clinical, biological, scientific, or health-related field
5+ years of practical experience in clinical trial administration (e.g., Inhouse CRA, CTA, site administration)
Strong knowledge of clinical studies and TMF functionality in accordance with study-specific plans and SOPs
Ability to work independently and manage multiple projects in a fast-paced environment
Preferred location: East Coast
Qualifications
- •Bachelor's degree or international equivalent in a clinical, biological, scientific, or health-related field
- •5+ years of practical experience in clinical trial administration (e.g., Inhouse CRA, CTA, site administration)
- •Strong knowledge of clinical studies and TMF functionality in accordance with study-specific plans and SOPs
- •Ability to work independently and manage multiple projects in a fast-paced environment
Benefits
Responsibilities
- •Assist in eTMF filing and administration, including document submission, review, and final collection
- •Create and maintain tracking tools and databases for operational data, including KPIs and quality metrics
- •Participate in project team meetings, prepare meeting minutes, and maintain action/decision logs
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