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Senior CTA (Supply) - Sponsor Dedicated

Role overview

Qualifications

  • University or college degree (biological or life science preferred), or certification in a related allied health profession
  • Understanding of ICH-GCP guidelines
  • Understanding of the clinical trial process
  • Good communication skills, oral and written

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
  • Update clinical trial databases (CTMS) and tracker

Key facts

  • Remote from: Turkey
  • Full time
  • Senior (5-10 years)
  • English

Other skills

  • Planning
  • Time Management
  • Problem Solving
  • Communication
  • Social Skills
  • Teamwork

About the company

Fortrea logo

Fortrea

Contract Research Organizations (CRO)

We are creative thinkers with decades of clinical trial experience who drive innovative solutions powered by insights from data and technology. As we tackle challenges in today’s world, we know that we need to be nimble and agile. That’s why we work side-by-side with our partners to eliminate inefficiencies from the process so we can help them deliver life-changing therapies faster for patients, caregivers and healthcare providers worldwide.

Company details

Company typeXLarge
IndustryContract Research Organizations (CRO)
Company size10001

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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, 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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Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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