Sponsor Dedicated Local Trial Manager based in Germany

Fortrea; Deutschland; Remote; EUR 60.000 - 90.000; Vollzeit

Zusammenfassung

Fortrea is looking for an experienced Clinical Project Manager to join their team. This home-based role involves overseeing clinical trials and ensuring regulatory compliance, making it ideal for candidates with a strong background in clinical research. Join Fortrea to expand your leadership capabilities and be part of impactful clinical research.

Leistungen

Flexible working arrangement

Opportunities for professional development

Access to mental health support

Qualifikationen

• Strong background in clinical research with experience in drug trials.
• 1-2 years in clinical project management within a CRO or Sponsor.
• Excellent German and English skills, both verbal and written.

Aufgaben

• Manage planning, execution, and completion of clinical trials.
• Serve as primary contact for clinical operations teams and vendors.
• Ensure compliance with GCP and regulatory requirements.

Kenntnisse

Problem Solving

Team Leadership

Effective Communication

Clinical Research

Risk Management

Regulatory Compliance

Bilingual (German and English)

Ausbildung

University/College Degree in Life Sciences

Certification in Allied Health Profession

Jobbeschreibung

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.

This role is for upcoming future opportunities that may arise at Fortrea.

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
  
• A t 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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