As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
Are you a dynamic leader passionate about driving clinical trials to success? We are looking for an experienced Clinical Trial Manager responsible for study oversight and delivery management (time, budget, quality)from start-up to closure in Germany. In this role, you’ll collaborate with sponsors, investigators and cross-functional teams to bring life-changing treatments to patients.

REQUIRED QUALIFICATIONS:

• Bachelor’s or Master’s degree required, preferably within Life Sciences or equivalent
• Thorough understanding of GCP, ICH Guidelines and Country regulatory environment
• Strong understanding of the clinical landscape and of clinical research processes, regulations and methodology
• Experience in leading or participating as an active member of cross functional teams, task forces, or local and global initiatives
• Ability of critical thinking and risk analysis
• Fluency in German and in English

WHAT WE OFFER:

• Work with an industry-leading sponsor and expand your leadership capabilities.
• Hybrid/remote options and a strong focus on work-life balance.
• Ongoing training, leadership programs and supportive work environment
  Join us in advancing groundbreaking clinical research. Apply today and be part of a team that makes a difference!
  

  LI-GQ1 #LI-Remote #LI-Hybrid

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.

KEY RESPONSIBILITIES:

• Manage clinical trial activities from start-up to close-out, ensuring adherence to timelines, budgets and quality standards.
• Serve as the primary liaison between sponsors, sites, and internal teams, ensuring seamless communication and issue resolution.
• Prepare and participate in Investigator Meetings and prepare material for Site Initiation Visits.
• Validate study related materials (i.e. protocol, ICF, patient material) and prepare country specific documents
• Review Site Monitoring visit reports and ensures timelines are met.
• Manage site relationships (includes CRO related issues)