
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.
🕒 March 14
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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.
• Provide medical monitoring for assigned projects • Function as medical representative on the project team • Provide medical consultation as required or requested to client/sponsor or to other Parexel service groups • Review all individual adverse experience reports for accuracy and clinical importance • Provide reports to FDA or other regulatory agencies and the sponsor on a periodic and regular basis • Review data listings of safety data, including adverse experiences, laboratory data, and vital signs data • Review documents written by various Parexel divisions for safety issues • Provide support for the preparation of clinical protocols, integrated clinical and statistical summary reports, and journal articles
• Medical Degree from an accredited institution • Board Certification / Fellowship in Oncology or equivalent training • 2+ years of experience in adult or pediatric oncology • Prior experience as a Medical Monitor, Industry Physician, Primary Investigator, or Sub-Investigator highly preferred
• Health insurance • 401(k) matching • Flexible work hours • Paid time off
Apply Now🕒 March 14
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