Job Description

CTA - Rare Disease Biotech

Job Description:

We are currently partnered with well-funded biotech with both clinical and commercial products on the market. 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.

Key Responsibilities:

• Maintain and manage the Trial Master File (TMF) and study documentation.
• Support the preparation and coordination of clinical trial meetings and submissions.
• Track study progress, patient enrollment, and site communications.
• Liaise with internal teams, CROs, and site personnel to ensure efficient trial operations.
• Ensure timely and accurate data entry and document filing.

Qualifications:

• Bachelor’s degree in life sciences or related field.
• 0–3 years of CTA experience in clinical research, preferably in rare disease or orphan indications.
• Strong organizational skills and attention to detail.
• Familiarity with GCP, ICH guidelines, and clinical trial processes.

If interested in this position, please reach out to tanya.kochan@meetlifesciences.com.

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