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Sponsor Dedicated Site Budget & Contract Specialist based in Switzerland

Fortrea·Switzerland·01.09.2026

 fortrea.wd1.myworkdayjobs.com

 
 
full_time80–100%
Required language
German professional, English professional
Job written in
English
Location
Switzerland
Type
Full-time

 

Fortrea, a firm dedicated to simplifying clinical trials and meeting worldwide regulatory standards, seeks a Sponsor Dedicated Site Budget & Contract Specialist who will operate remotely from Switzerland. The role sits within the FSP team and supports a prominent sponsor in moving forward innovative, life‑changing therapies. In this position you will draft, negotiate and oversee site agreements, confidentiality pacts and indemnity letters for clinical studies, while guaranteeing alignment with SOPs, regulatory rules and contractual duties. You will keep contract status current in tracking tools, flag any issues to leadership, and aid internal review and approval before external distribution. Close collaboration with study teams, legal counsel and project managers will ensure smooth contract execution, and you will maintain both electronic and paper files with precision. Regular updates on progress will be provided to managers and study groups, and you will contribute to ongoing improvements of departmental workflows. The ideal candidate holds a bachelor’s degree—preferably a law qualification such as an LLB or JD—or equivalent experience, and brings two to four years of experience in contract negotiation, clinical research, or a related arena. A solid grasp of ICH GCP guidelines and clinical research processes is essential, as are strong negotiation, communication and organisational abilities. You must be capable of independent work, juggling several priorities in a rapid environment, and be proficient with Microsoft Office and contract‑tracking platforms. Fluency in both German and English is required. Fortrea offers a competitive salary with performance incentives, flexible remote work options and opportunities for professional development within a collaborative, innovative setting. The role provides exposure to cutting‑edge clinical research projects and the chance to make a tangible impact on the advancement of life‑saving therapies.

 

 

 

 

 

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