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, study coordinator).
Previous experience as a CTA or in a similar position.
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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Learn more about our EEO & Accommodations request here.
Skills Required
- University or college degree, preferably in biological or life sciences, or certification in a related allied health profession
- Understanding of ICH-GCP guidelines
- Understanding of the clinical trial process
- Minimum 1.5 years of industry experience in a related role, such as IHCRA, CTA, or study coordinator
- Previous experience as a CTA or in a similar position
- Experience in clinical research supply management processes
- Good planning, organization, time management, and problem-solving skills
- Good oral and written communication skills
- Ability to work efficiently and effectively in a matrix environment
What We Do
Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.
