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Senior CRA II Sponsor dedicated Türkiye

Job in Indianapolis, Hamilton County, Indiana, 46262, USA
Listing for: Fortrea
Full Time position
Listed on 2026-10-02
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 90000 - 120000 USD Yearly USD 90000.00 120000.00 YEAR
Job Description & How to Apply Below
Position: Senior CRA II Sponsor dedicated based in Türkiye
Location: Indianapolis

Join Fortrea as a Senior Clinical Research Associate II in Türkiye within a sponsor-dedicated model, where you will work exclusively with a leading global biopharmaceutical partner.

In this role, you will support the delivery of high-quality clinical trials across innovative therapies, building strong site relationships and ensuring excellence in study execution.

Working in this model offers close collaboration with the sponsor’s teams, strong study ownership, and the opportunity to contribute directly to advancing cutting-edge treatments for patients worldwide.

Core responsibilities:
  • Act as primary contact for assigned clinical trial sites, building strong, collaborative relationships
  • Manage site lifecycle from start-up through monitoring and close-out, ensuring delivery to timelines and quality standards
  • Conduct on-site and remote monitoring, identifying risks and driving timely issue resolution
  • Ensure compliance with study protocol, ICH-GCP, and local regulatory requirements
  • Oversee site performance including data quality, recruitment, training, and documentation completeness
  • Support study execution (e.g. feasibility, site activation, investigator meetings, audit readiness)
  • Collaborate cross-functionally to implement site strategies and ensure successful trial delivery
Required Qualifications:
  • Bachelor’s degree in Life Sciences or equivalent experience
  • ≥5 years’ experience in clinical research, including site monitoring/site management
  • Proven experience in Oncology , Ophthalmology, Gene Therapy or similar therapeutic area
  • Strong knowledge of ICH-GCP, regulatory requirements, and clinical trial processes
  • Solid problem-solving and critical thinking skills
  • Proficiency in Turkish and in English
  • Willingness to travel

Learn more about our EEO & Accommodations request here.

Position Requirements
10+ Years work experience
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