When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Key Accountabilities: Operational Execution Coordinate and lead a project team to successful completion of a project within timelines and budget Interact with clients as key contact with regard to statistical and contractual issues Perform QC of derived datasets, tables, figures and data listings produced by other members of the department Check own work in an ongoing way to ensure first time quality Understand and apply advanced statistical methods Lead production and quality control of randomizations, analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents Provide a supporting role as a non-voting independent statistician providing data and analysis for DMC review Travel to, attend, and actively contribute to all kind of client meetings as appropriate (e.g. discussing analysis concepts, presenting, discussing and interpreting study results) Business Development Support of Business Development, e.g. by actively contributing to study design considerations in internal and client meetings, providing and discussing sample size scenarios, support of budget and proposal development, attending and preparing bid defense meetings for potential studies, programs of work and FSPs General Activities Additional responsibilities as defined by supervisor/manager. Skills: Good analytical skills Good project management skills Professional attitude Attention to detail Thorough understanding of statistical issues in clinical trials Prior experience with SAS programming required Ability to work independently Good leadership skills Good business awareness/ business development Willingness to work in a matrix environment and to value the importance of teamwork Knowledge and Experience: PhD in Statistics or related discipline with some experience or MS in Statistics or related discipline with significant experience The knowledge of pharmacokinetic data is an advantage Competent in written and oral English in addition to local language Education: PhD in Statistics or related discipline, MS in Statistics or related discipline Required Qualifications: • Study design expertise, specifically for IIT and RWE studies • Protocol development experience • Proficiency in SAS and R programming • Excellent communication skills with relevant stakeholders • Available for interviews soon Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart.™

Senior Biostatistician.

more at Parexel.

Statistical Programmer I

Job Posting Title Clinical Operations Leader / 臨床開発部クリニカルオペレーションズリーダー

Site Monitor II - FSP

similar roles.

Production Supervisor

Fleet Team Driver