
10,000+ employees
Founded 1983
âïž Healthcare Insurance
đ§Ź Biotechnology
đ Pharmaceuticals
đ° Venture Round on 1990-01
Healthcare Insurance âą Biotechnology âą 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.
đ 2 days ago
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10,000+ employees
Founded 1983
âïž Healthcare Insurance
đ§Ź Biotechnology
đ Pharmaceuticals
đ° Venture Round on 1990-01
Healthcare Insurance âą Biotechnology âą 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.
âą Oversight of activities âą Evaluate the intent of the study concept and make informed recommendations based on scientific review âą Effectively communicate with key stakeholders through the initial viability/feasibility concept phase âą Utilize tools (e.g. Medidata, Symphony) to generate data to satisfy feasibility/viability requests âą Author reports to inform project teams of assessments âą Collaborate with cross-functional teams to evaluate study concepts and deliver comprehensive feasibility reports
âą Minimum 5 years of relevant experience âą Excellent knowledge of GCP and regulations âą Scientific understanding for the areas of interest for the client to help support effective viability considerations âą Ability to author scientific documentation to support viability consideration. âą Utilization of software applications to support data collection and clear interpretation of this data to assist in the evaluation of the study viability. âą Experience of team management
âą Complies with required training curriculum âą Completes timesheets accurately as required âą Submits expense reports as required âą Updates CV as required
Apply Nowđ 2 days ago
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