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.
Principal Site Contracts Associate
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 Draft, review and negotiate site agreements including clinical study agreements, service agreements, and team member agreements âą Provide context to comments received from sites based on legal and business framework âą Manage the contract execution process âą Develop and maintain positive relationships with clinical trial sites âą Track and report on the statuses of site contracting activities
đŻ Requirements
âą 8+ years of experience in site contracting or a related field within the CRO industry âą Strong negotiation and organizational skills âą Proficient in Microsoft Office Products specifically, Excel, Word, and PowerPoint âą Ability to mentor and motivate junior staff âą Fluent in written and spoken English; command of additional languages is beneficial
đïž Benefits
âą Health insurance âą Retirement plans âą Professional development âą Paid time off
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