Freelance Site Contract Manager

Job not on LinkedIn

🔥 13 hours ago

🇩🇪 Germany – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

👻 Ghost score 10%

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Immatics

WebsiteLinkedInAll Job Openings

201 - 500 employees

Founded 2000

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

Healthcare • Biotechnology • Pharmaceuticals

Immatics is a biotechnology company focused on developing targeted immunotherapies for cancer patients, particularly in treating solid tumors. The company combines the discovery of cancer immunotherapy targets with the development of specific T cell receptors to enable a robust immune response. Immatics' pipeline includes Adoptive Cell Therapies and TCR Bispecifics, and it collaborates with global leaders in the pharmaceutical industry. The company's mission is to advance its therapies to improve the lives of cancer patients, and it maintains a strong commitment to innovation in immunotherapy technologies.

📋 Description

• Independently manage Clinical Trial Agreements (CTAs) and site budgets for clinical trial sites in Germany and Spain • Prepare, review, negotiate, and finalize CTAs, site budgets, and amendments • Lead contract and budget negotiations with clinical trial sites, including university hospitals and legal departments • Develop site budgets using internal and external benchmarks and approved study assumptions • Apply country-specific contracting requirements and seek legal or local support where needed • Identify and mitigate contractual risks, negotiation challenges, and potential impacts on study timelines • Manage contracting timelines, prioritize activities, and drive timely execution • Apply approved negotiation positions and escalate exceptions as required • Coordinate with sites, study teams, Legal, and other stakeholders • Review contract redlines, resolve comments within authority levels, and support other negotiators • Maintain accurate contracting records and provide transparency on status, risks, and next steps

🎯 Requirements

• Experience in clinical trial site contracting within the pharmaceutical, biotechnology, or CRO industry • Proven track record of independently negotiating and executing CTAs and site budgets in Germany and Spain • Strong knowledge of relevant clinical trial regulations and country-specific requirements • Excellent communication skills in German and English • Experience in oncology, cell therapy, study start-up activities, sponsorship and CRO environments considered an advantage • Additional language skills and broader European contracting expertise considered an advantage

🏖️ Benefits

• Temporary, project-based freelance engagement • Work packages assigned based on business demand, with varying scope and volume • Equal opportunity employment and diversity and inclusion commitment

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