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.
Senior Clinical Research Associate
đ„ 0 minutes ago
đ Check your resume score for this job
Improve your chances of getting an interview by checking your resume score before you apply.
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 Set up and oversee a study âą Complete study status reports âą Maintain study documentation âą Participate in the submission of protocols and consent documents for ethics/IRB approval âą Assist in the preparation of regulatory submissions as requested
đŻ Requirements
âą Bachelor's degree in a life science or related discipline âą Minimum of 5 years' experience in independent site monitoring âą At least 2 years in oncology âą Understanding of ICH GCP Compliance âą Excellent time management and social skills âą Highly motivated with a phenomenal eye for detail âą Ability to travel domestically and internationally approximately 65%-75% of working time âą Current driverâs license required
đïž Benefits
âą Premium salary âą Attractive benefits âą Medical care plan: Health, Dental & Vision âą Life Assurance âą Excellent work environment âą Culture of teamwork and collaboration âą Excellent training
Apply NowSimilar Jobs
đ April 1
Senior Product and Market Research Specialist shaping product portfolios at Beckman Coulter Life Sciences. Collaborating on customer-focused research initiatives and cross-functional teamwork to drive innovation.
đŁïžđ«đ· French Required
