Overview
An experienced Site Contract Associate I/II is needed to support clinical trial site agreements in Serbia. This is a homebased role for candidates living in Serbia. The role requires business-level fluency in German, as well as Serbian and English.
Responsibilities
- Draft and negotiate contracts, including clinical study agreements, service agreements, team member agreements, and related documents.
- Interpret site feedback within local legal and business frameworks to guide internal decision-makers.
- Ensure compliance with ICH-GCP, local laws, and internal guidelines.
- Serve as the communication hub between internal teams, site staff, and external partners.
- Manage the full contract lifecycle, from first draft through final signature and archival.
- Build and maintain relationships with clinical trial sites and internal stakeholders.
- Identify risks early and collaborate with the Site Contract Lead to resolve them.
- Track contract progress in real time and keep teams informed.
- Drive process improvements to make contracting faster, clearer, and more efficient.
Requirements
- Strong negotiation skills and diplomacy to navigate complex conversations.
- Excellent written and verbal communication.
- Strong problem-solving and analytical thinking.
- Ability to work confidently in a virtual, global team.
- Grace under pressure and a polished, professional presence.
- Strong attention to detail and commitment to quality.
- Fluency in GERMAN required.
- Solid proficiency in MS Office (Word, Excel, PowerPoint).
- Homebased role: must be living in Serbia.
Education & Experience
- Bachelor’s degree in law, economics, business, social sciences, or a related field.
- Level I: no prior industry experience required.
- Level II: experience in Life Sciences.
Compensation & Benefits
- Not specified in the provided job description.
Location
- Serbia (homebased). Must be living in Serbia.
- Languages: Business level fluency in GERMAN required, plus Serbian and English.