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Clinical Trial Assistant
166026
Posted:
10/05/2025
- 60000 USD - 90000 USD
- San Francisco Bay Area, United States
- Permanent
Job Description:
We are currently partnered with a well-funded biotech company with both clinical and commercial products in their pipeline. They are seeking a detail-oriented Clinical Trial Assistant (CTA) to support the planning, execution, and oversight of clinical trials focused on rare diseases. The CTA will assist with study documentation, trial tracking, vendor coordination, and regulatory submissions, ensuring compliance with GCP, SOPs, and applicable regulations.
This is an opportunity to join a collaborative, patient-centric company culture where your work will have a meaningful impact. This role offers strong potential for career growth, development, and high visibility within the organization.
Key Responsibilities:
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Maintain and manage the Trial Master File (TMF) and study documentation.
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Support the preparation and coordination of clinical trial meetings and submissions.
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Track study progress, patient enrollment, and site communications.
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Liaise with internal teams, CROs, and site personnel to ensure efficient trial operations.
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Ensure timely and accurate data entry and document filing.
Qualifications:
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Bachelor’s degree in life sciences or related field.
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0–3 years of CTA experience in clinical research, preferably in rare disease or orphan indications.
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Strong organizational skills and attention to detail.
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Familiarity with GCP, ICH guidelines, and clinical trial processes.
Tanya Kochan
Account Manager