A company is looking for a Clinical Trial Assistant (Remote & Full-Time).
Key Responsibilities
Maintain and manage the Trial Master File (TMF) for accuracy and inspection readiness
Act as a primary point of contact for external vendors and monitor their deliverables
Assist in study start-up, conduct, and close-out activities across multiple trials
Required Qualifications
Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field
Minimum of 3 years of experience in a CTA or similar role, preferably in biotech, pharma, or CRO
Experience working in small company environments or with multiple external vendors
Familiarity with Phase I-III clinical trials
Strong understanding of ICH-GCP, clinical trial processes, and regulatory requirements
Clinical Trial Assistant • Beaumont, Texas, United States