
10,000+ employees
Founded 1983
💼 Consulting
🏥 Healthcare
📦 Logistics
💰 Venture Round on 1990-01
Consulting • Healthcare • Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
🔥 3 hours ago
🗣️🇮🇹 Italian Required
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10,000+ employees
Founded 1983
💼 Consulting
🏥 Healthcare
📦 Logistics
💰 Venture Round on 1990-01
Consulting • Healthcare • Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
• Draft and negotiate 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 • Act as the communication hub between internal teams, site staff, and external partners • Manage the full contract lifecycle from first draft to final signature and archival • Build relationships with clinical trial sites and internal stakeholders • Identify risks early and collaborate with the Site Contract Lead to resolve them • Track progress in real time and keep teams informed • Drive process improvements to make contracting faster, clearer, and more efficient
• Fluency in Italian, Serbian, and English • Strong negotiation skills and diplomacy • Excellent written and verbal communication • Problem-solving and analytical thinking • Ability to work confidently in a virtual, global team • Grace under pressure and polished, professional presence • Strong attention to detail and commitment to quality • Solid proficiency in MS Office (Word, Excel, PowerPoint) • Bachelor’s degree in law, economics, business, social sciences, or a related field • No prior industry experience required for Level I • Level II requires experience in Life Sciences
• Homebased role • Virtual, global team environment
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