Clinical Trial Assistant (Supply) - Sponsor Dedicated
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
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Clinical supply & non‐clinical supply management, in collaboration with other country roles
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Collate, distribute/ship, and archive clinical documents
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Manage Labeling requirements and coordinate/sign translation change request
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Prepare documents and correspondence
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Ensure collection and distribution of study tools and documents
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Update clinical trial databases (CTMS) and tracker
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Assist with eTMF reconciliation
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Document proper destruction of clinical supplies.
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Execute eTMF Quality Control Plan
Qualifications (Minimum Required)
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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).
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Understanding of ICH-GCP guidelines.
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Understanding of the clinical trial process.
Experience (Minimum Required)
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A minimum of 1.5 years of industry experience in a related role (e.g., IHCRA, CTA, Supply CTA ).
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Experience in clinical research supply management processes preferred.
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Good planning, organization, time management and problem-solving skills.
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Good communication skills, oral and written.
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Works efficiently and effectively in a matrix environment.
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