Fortrea is recruiting an experienced Clinical Project Manager with valuable expertise in Oncology. In this role, you will ensure the successful execution of clinical studies on a local level, while maintaining high-quality standards and regulatory compliance.
Key responsibilities:
Manage the planning, execution, and completion of clinical trials, ensuring timelines, budget, and quality expectations are met.
Serve as primary point of contact for clinical operations teams, vendors and other external partners, overseeing cross-functional teams
Identify and mitigate risks to ensure smooth study progress
Ensure compliance with GCP, ICH guidelines and German EU regulatory requirements
Supports local and regional strategy development consistent with long-term corporate needs
Qualifications:
University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution, nursing certification, medical or laboratory technology (Fortrea may consider relevant and equivalent experience in lieu of educational requirements).
Strong background in clinical research, including several years of experience working on drugs trials and interventional studies
At least 1-2 years experience in clinical project management within a CRO or Sponsor environment
Ability to lead teams, communicate effectively, and solve problems proactively
Excellent German and English skills verbal and written
What We Offer:
Home-Based role with flexible working arrangement.
Opportunities for professional development, mentorship, and career progression.
Work with an industry-leading sponsor and expand your leadership capabilities.
Thanks to our ERGs (Employee Resource Groups), join divers communities that foster inclusion, professional development, and networking.
Access to mental health support, wellness initiatives, and fitness programs.
We welcome applications from all qualified candidates. Apply today to be part of impactful clinical research!
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Learn more about our EEO & Accommodations request here.
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