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.
Biostatistician II
đ March 2
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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 Coordinate and lead a project team to successful completion of a project within timelines and budget âą Interact with clients as key contact with regard to statistical and contractual issues âą Perform QC of derived datasets, tables, figures and data listings produced by other members of the department âą Check own work in an ongoing way to ensure first time quality âą Understand and apply advanced statistical methods âą Lead production and quality control of randomizations, analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents âą Provide a supporting role as a non-voting independent statistician providing data and analysis for DMC review âą Travel to, attend and actively contribute to all kind of client meetings as appropriate
đŻ Requirements
âą PhD in Statistics or related discipline with some experience or MS in Statistics or related discipline with significant experience âą Prior experience with SAS programming required âą Competent in written and oral English in addition to local language
đïž Benefits
âą Professional attitude âą Attention to detail
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