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.
- PhD or MS in Statistics or related discipline with relevant experience of 5 - 8 years.
- Statistician for Phase I-IV clinical studies in different therapeutic areas.
- Provide statistical inputs in protocol, database design, manuscript writing and overall conduct of the study.
- Perform sample size calculation and generate randomization schedule as per study requirement.
- Write and review statistical analysis plan, statistical sections in protocol, clinical study reports for regulatory submissions and journal manuscripts.
- Perform all statistical activities including mock shell development, prepare/review safety and efficacy TLFs, qcing primary endpoints related datasets/outputs using double programming in SAS.
- Prepare and review key portion of clinical study report and academic research manuscript, including sections related to data handling and statistical methodology, patient accountability, efficacy and safety results
- Prepare study timelines and execute them for the timely submission of deliverables.
Top Skills
What We Do
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.
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