Clinical Trial Assistant (Supply) - Sponsor Dedicated

FTTRK Fortrea Turkey Klinik Araştırma Limited Şirketi (Fortrea Turkey Clinical Study Limited Company; Fatih; Hybrid; TRY 900,000 - 1,500,000; Full time

Job summary

Fortrea Turkey Clinical Study Limited Company is seeking a Senior CTA (Supply) to join its sponsor-dedicated (FSP) team. This permanent, full-time role offers a hybrid work arrangement in Istanbul and Ankara, Turkey, with opportunities for future roles as the program grows.

Responsibilities span clinical and non-clinical supply management, document handling, labeling coordination, and eTMF activities, with exposure to diverse disease areas and clear paths for career progression.

Qualifications

• University degree or allied health certification from an accredited institution.
• Understanding of ICH-GCP guidelines.
• Understanding of the clinical trial process.

Responsibilities

• Clinical supply & non-clinical supply management with country teams.
• Collate, distribute/ship, and archive clinical documents.
• Manage labeling requirements and coordinate translation changes.
• Prepare documents and correspondence.
• Ensure collection and distribution of study tools and documents.
• Update CTMS and trial trackers.
• Assist with eTMF reconciliation.
• Document proper destruction of clinical supplies.
• Execute eTMF Quality Control Plan.

Skills

ICH-GCP

Communication

Problem-solving

Time management

Matrix environment

Education

Biological or life sciences degree

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.

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