Sponsor Dedicated Local Trial Manager based in Germany

Fortrea; Deutschland; Remote; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A global clinical research organization is seeking an experienced Clinical Project Manager to manage and execute clinical trials in oncology while ensuring compliance with regulatory standards. The role offers a flexible home-based working arrangement and opportunities for professional development. Ideal candidates have a strong background in clinical research, effective communication skills, and are proficient in German and English.

Leistungen

Flexible working arrangements

Professional development opportunities

Mental health support

Access to fitness programs

Qualifikationen

• Strong background in clinical research with experience in drug trials.
• At least 1-2 years experience in clinical project management.
• Ability to lead and manage cross-functional teams.

Aufgaben

• Manage planning and execution of clinical trials.
• Serve as primary point of contact for teams and vendors.
• Ensure compliance with GCP, ICH guidelines and local regulations.

Kenntnisse

Communication skills

Problem-solving

Team leadership

German language proficiency

English language proficiency

Ausbildung

University degree in life science or equivalent

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.

Please note 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 drug 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!

Learn more about our EEO & Accommodations request here.