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.
Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
3 days ago
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.
Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
• Responsible for study, regional or specific country level activities from study start-up through conduct and study close. • Responsible for study management aspects of assigned studies, including vendor and budget management. • Regional/Country/Study level implementation of Startup and Site Activation Plans. • Responsible for communication with the local team and internal stakeholders and CRO partner as applicable to ensure efficient and timely study delivery of the agreed plans. • Responsible for study and/or country vendor management and oversight including follow up and coordination of vendor deliverables.
• Minimum of 5 years of relevant global/regional clinical trial management experience. • Excellent leadership, communication, and organizational skills. • Able to multi-task under limited direction and on own initiative. • M.S/ M.A / Ph.D or B.A/ B.S / nursing degree is essential. • Prior and demonstrable experience working at a senior level within Study Start-Up.
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