Clinical Trial Assistant (Supply) - Sponsor Dedicated
Company: Fortrea
- Location: Istanbul, Türkiye
- Work mode: Hybrid
- Seniority: Mid level
- Employment type: Full-time
- Posted: 8 days ago
- Offer language: English
Job description
We are recruiting for our sponsor-dedicated (FSP) business in Türkiye and are seeking to hire a Senior CTA (Supply) on a permanent, full-time contract.
This hybrid position is offered in Istanbul and Ankara and is for future roles which may arise.
Our positions offer excellent exposure to a range of disease areas, and a real opportunity for career progression and promotion in time.
Summary Of Responsibilities
- Clinical supply & non‐clinical supply management, in collaboration with other country roles
- Collate, distribute/ship, and archive clinical documents
- Manage Labeling requirements and coordinate/sign translation change request
- Prepare documents and correspondence
- Ensure collection and distribution of study tools and documents
- Update clinical trial databases (CTMS) and tracker
- Assist with eTMF reconciliation
- Document proper destruction of clinical supplies.
- Execute eTMF Quality Control Plan
Qualifications (Minimum Required)
- University or college degree (biological or life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure, medical or laboratory technology).
- Understanding of ICH-GCP guidelines.
- Understanding of the clinical trial process.
Experience (Minimum Required)
- A minimum of 1.5 years of industry experience in a related role (e.g., IHCRA, CTA, Supply CTA ).
- Experience in clinical research supply management processes preferred.
- Good planning, organization, time management and problem-solving skills.
- Good communication skills, oral and written.
- Works efficiently and effectively in a matrix environment.
Learn more about our EEO & Accommodations request here.
