
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
Healthcare Insurance • Biotechnology • Pharmaceuticals
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.
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10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
Healthcare Insurance • Biotechnology • Pharmaceuticals
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.
• Accountable for the operational and scientific oversight, the set-up, execution and delivery of assigned clinical trials at the local level. • Contribute to delivery of the pipeline through accurate planning and efficient execution of trials. • Perform monitoring visits if the need arises. • Provide leadership and direction to the wider trial team. • Accountable for the overall success and delivery of assigned clinical trial/s according to defined milestones and key performance indicators. • Verify the trial is conducted in compliance with GCP-ICH, local/global regulations. • Create, manage, and review the trial budget and provide timely budget updates based on trial changes. • Perform trial-specific training of internal and external partners. • Plan and co-ordinate operational feasibility of trial timelines.
• Minimum of 5 years of relevant clinical trial management experience. • Experience of managing oncology studies is preferred. • Experience managing outsourced trials or CRO Management Vendor 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.
• N/A
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