As a Biostatistician at Parexel you’ll work on a variety of projects, while collaborating with our global team of experts. You’ll be able to develop your statistical skills, gain exposure to multiple therapeutic areas, become involved in business development activities, and have the opportunity to grow and develop your career within a flexible working environment. You’ll also contribute to research design and analytical strategies, provide input into protocols, and develop and review statistical analysis plans.
Check out the top traits we're looking for and see if you have the right mix.
Opportunity to learn and grow through a performance and development goal-setting program.
We value work-life balance. We try and keep regular hours and a flexible working enviroment.
Work with industry leaders and subject matter experts.
The ability to innovate, ask “what if” and try new solutions without fear of failure.
Utilize Parexel’s industry leading clinical systems and solutions
Strong mentors with depths of experience working for global health authorities.
The position serves as the primary statistical role with technical accountabilities plus coaching, mentoring and developing other statisticians and programmers.
The Principal Biostatistician is expected to provide broad statistical support, contribute strategically to project decisions with a focus on pre-study planning, protocol development, sample size / power calculations, Statistical Analysis Plan preparation/ review, data quality reviews, development of tables / listings / figures, preparation / mapping of clinical study data for regulatory submission.
The Principal Biostatistician is expected to have an understanding of advanced statistical methods and to research complex and innovative statistical approaches (e.g, modeling and simulation, adaptive design / Bayesian statistics) and mentor junior staff in the use of these approaches.
The professional will participate in meetings and teleconferences and also provide consulting, interpretive and analytical support to Clients.
Review publications and clinical study reports. Assist with the technical details of client proposal documents.
Represent PAREXEL at client marketing and technical meetings.
Required skills and experience:
Ph.D. degree or equivalent in statistical science, mathematical analysis or related field plus 4 years relevant experience or a master’s degree plus 6 years relevant experience
Comprehensive knowledge of statistical theory and methods and demonstrated ability to apply it to all phases of clinical trials
Expertise in SAS programming including statistical analysis, data manipulation and scientific graphing.
Experience in all tasks of a Trial Statistician
Proven knowledge in Statistics and its applications to clinical trials
Proven knowledge of statistical software packages
Good communication and presentation skills
Possess strong negotiation, diplomacy, team leadership skills and excellent organizational ability
Excellent interpersonal, verbal and written communication skills
Ability to identify and address issues proactively in a timely manner
Ability to make appropriate decisions in ambiguous situations
Carefully weighs the priority of project tasks and directs team accordingly
Excellent computer literacy
Demonstrate a sound knowledge of all relevant regulations, including GCP
PAREXEL is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.