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.
Our FSP Department is looking for a Site Contract Specialist based in Germany and responsible for the oversight and negotiation of site agreements for a variety of clinical trials. In this critical role, you will be in charge of the the end-to-end management of budgeting and contracting for Study Teams.

REQUIRED QUALIFICATIONS:

• Bachelor’s degree required preferably within life sciences or equivalent
• 2 or more years experience negotiating legal and/or financial agreements, preferably in pharmaceutical industry clinical trials or years of industry related experience in clinical operations
• Strong negotiation and interpersonal skills including strong conflict resolution skills
• Working knowledge of clinical trial start-ups and finance cycles including knowledge of site needs and perspective
• Fluency in German and English

WHAT WE OFFER:

• Gain exposure to complex, high-impact clinical trials
• Hybrid/remote options, work-life balance, and team-oriented culture
• Training programs and mentorship
• Comprehensive benefits package to support your physical, financial, and emotional well-being.
  Apply today and be part of a team driving innovation!
  

  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 the end-to-end process for executing Clinical Trial Agreements with investigator sites
• Prepare contract documents and negotiate financial and legal aspects of agreements with sites, Institutions or vendor personnel.
• Act as key liaison between sponsor, sites, legal teams and clinical operations.
• Identify bottlenecks in contract execution and propose solutions to enhance efficiency.
• Ensure contracts are executed in alignment with trial deliverables and priorities
• May support preparing invoices/payments due reports and managing, tracking and executing payments to investigator sites.