Job Description
Come Join Our Growing Team! Are you ready to embark on an exhilarating journey with a team that's passionate about making a difference? Look no further - Pharmaron is thrilled to invite you to join us as our newest
Principal Statistician with our team
in Somerset, New Jersey. Hybrid work is available but must be able to commute to site.
What The Job Entails: - Develop and/or review statistical sections of a study protocol with high complexity independently.
- Perform and/or verify sample size and statistical power calculation for typical trial designs.
- Develop statistical analysis plans, table/listings/figures mock-ups and statistical analysis reports for a study with different complexity.
- Act as a randomization statistician to develop the randomization protocol and generate the randomization schedule.
- Attend client meetings including, but not limited to, project kick-off meetings, resource/timelines discussions, bid defenses, blind data review meetings etc.
- QC/review case report form and other DM documents including, but not limited to edit check specifications, data review plan, data transfer specification and etc.
- QC/review programming deliverables including, but not limited to programming specifications, analysis datasets and TLFs and etc. to ensure to meet the analysis requirements. CRO-GP-FM-002 Version: 2.0 Released date: 2022.12.07 Job Descriptions Effective date: 2022.12.21 Confidential and Proprietary 2 / 3
- Mentor statistical programmers and Biostatisticians
- Ensure all activities in accordance with internal and external quality standards, SOPs/WIs, ICH-GCP and/or any other applicable local and international regulations, guidelines and industry standards.
What We're Looking For: Skills and Experience:
- Master's degree or PhD in Statistics, Biostatistics or related field,
- 5 plus years relevant experience in clinical trial statistics
- Familiar with SAS Base, SAS/Macros, SAS/Graph, SAS/Stat and reporting process.
- Demonstrated understanding and insight in statistics, drug development process and relevant FDA regulations.
- Demonstrated ability to identify areas of statistical research in improving the design, analysis and reporting of clinical study.
- Strong oral and written communication skills, with the ability to communicate effectively internally and with clients.
- Demonstrated capability to effectively manage multiple projects.
Why Pharmaron? Pharmaron stands as a leading force in the life sciences industry, offering premier R&D services to partners across the globe. With a workforce of over 20,000 professionals and operations spanning China, the U.S., and the U.K., Pharmaron is committed to delivering innovative R&D solutions that drive advancements in healthcare
Collaborative Culture: You'll thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners and collaborators.
Rewards and Recognition: As part of our commitment to your well-being, we offer a comprehensive benefits package, including medical, dental, and vision insurance with significant employer contributions. Planning for your future is made easier with our 401k plan and employer match. Plus, you'll have access to an Employee Assistance Program to support you in work and life.
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
#LI-ZS1
Job Tags
Local area,