Site Contracts Associate I/II - Additional Languages Preferred

Parexel is a global leader in clinical development, dedicated to improving world health through innovative solutions. As a Site Contract 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-making.
• Ensuring full compliance with ICH-GCP standards, local regulations, 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

• Bachelor’s degree in law, economics, business, social sciences, or a related field.
• Strong negotiation skills with the ability to navigate complex professional conversations.
• Fluency in English and Polish, with proficiency in an additional language being highly preferred.
• Excellent analytical thinking and problem-solving capabilities.
• Solid proficiency in MS Office applications including Word, Excel, and PowerPoint.

What we offer

• The opportunity to work in a fully remote environment within a global, collaborative team.
• A meaningful role where your work directly contributes to the development of new therapies for patients.
• Professional growth opportunities within a leading organization in the life sciences industry.
• A supportive culture that values empathy, precision, and commitment to making a difference.