Fortrea

Senior CRA II Sponsor Dedicated based in Munich, Düsseldorf or Berlin regions

Fortrea  •  Munich, DE (Remote)  •  1 day ago
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Job Description

Join Fortrea as a Senior Clinical Research Associate II 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 German and in English
  • Willingness to travel
Join Fortrea and take ownership of clinical trial sites across innovative therapies, playing a critical role in delivering high-quality data and accelerating drug development. This role offers strong autonomy, cross-functional collaboration, and exposure to cutting-edge clinical research.
If you are passionate about advancing clinical research and want to grow your expertise in a sponsor-dedicated environment, we encourage you to apply and join us in making a meaningful impact on patients’

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Fortrea

About Fortrea

Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) dedicated to providing innovative clinical development solutions to the life sciences industry. With over 30 years of clinical research experience, Fortrea has evolved from Covance and Labcorp into a pureplay CRO built for biotech, biopharma, medical device and diagnostic innovators.

Fortrea collaborates with both emerging and established companies to deliver agile, fit-for-purpose full service (FSO), functional service (FSP) and hybrid solutions. Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in more than 20 therapeutic areas.

Operating in approximately 100 countries, our diverse and talented team brings scientific rigor, operational excellence, and a strong investigator site network to every trial. By combining the best of our legacy experience with forward-thinking innovation, Fortrea brings predictability to clinical trial execution and helps transform aspirations into outcomes.

Together, exceptional is possible.

Learn more at Fortrea.com

Industry
Biotech & Life Sciences
Company Size
10,000+ employees
Headquarters
Research Triangle Park, NC
Year Founded
Unknown
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