Parexel is a global leader in clinical development, dedicated to improving world health through innovative solutions. As a Site Contracts Associate, you will play a vital role in the clinical trial process by managing the agreements that enable life-changing research to move forward.
Key responsibilities
- Drafting and negotiating clinical study agreements, service agreements, and related legal documentation.
- Interpreting site feedback within local legal and business frameworks to guide internal decision-makers.
- Ensuring full compliance with ICH-GCP, local laws, and internal company guidelines.
- Acting as a central communication hub between internal teams, clinical trial sites, and external partners.
- Managing the complete contract lifecycle from initial drafting through to final signature and archival.
Requirements
- Fluency in German, Polish, and English is mandatory for this position.
- Bachelor’s degree in law, economics, business, social sciences, or a related field.
- Strong negotiation skills and the ability to navigate complex professional conversations.
- Excellent analytical thinking and problem-solving capabilities.
- Proficiency in MS Office applications including Word, Excel, and PowerPoint.
What we offer
- An entry-level opportunity with significant room for professional growth and development.
- The chance to work in a fully remote environment within a global, collaborative team.
- Meaningful work that directly contributes to the development of new therapies for patients.
- A supportive culture focused on empathy, precision, and making a tangible difference in healthcare.