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.

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