Parexel
10,000+ employees
Founded 1983
âïž Healthcare Insurance
𧏠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.
Local Study Associate Director
đ„ 0 minutes ago
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Parexel
10,000+ employees
Founded 1983
âïž Healthcare Insurance
𧏠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 Description
âą Leads Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies âą Ensures that sites are identified, qualifications performed, set up, initiated, monitored, and closed âą Coordinates the site selection process by identifying potential sites/investigators âą Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction) âą Oversees monitoring activities from site activation to study closure âą Proactively identifies risks and facilitates resolution of complex study problems
đŻ Requirements
âą Minimum 3 years of experience in Development Operations (CRA, SrCRA) or related fields âą Good knowledge of international guidelines ICH GCP and relevant local regulations âą Bachelor's degree in related discipline, preferably in life science, or equivalent qualification âą Excellent project management skills âą Proficient in written and spoken English language required âą Fluency in local language(s) required
đïž Benefits
âą Education reimbursement âą Professional development opportunities âą Flexible working arrangements
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