
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
đź’Š Pharmaceuticals
đź’° 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
đź’Š Pharmaceuticals
đź’° 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.
• The CRA works in close collaboration with other CRAs and the Local Study Team to ensure that study commitments are achieved in a timely and efficient manner • Acts as the main contact with the study site and has the responsibility for monitoring study conduct • Responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies • Confirms that site staff have completed and documented the required training appropriately, including ICH-GCP training • Ensures that all study documents under their responsibility are available and ready for final archiving • Collaborates with local Medical Science Liaisons as directed by LSAD or line manager
• Bachelor’s degree in related discipline, preferably in life science • Excellent attention to detail • Good written and verbal communication skills • Good collaboration and interpersonal skills • Good negotiation skills • Proficient in written and spoken English language required • Fluency in local language(s) required • Basic knowledge of GMP/GDP • Good medical knowledge and ability to learn relevant Client Therapeutic Areas • Ability to travel nationally/internationally as Required
• Health insurance • Retirement plans • Paid time off • Flexible work arrangements • Professional development • Bonuses • Stock options • Equipment allowances • Wellness programs
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