Senior Biostatistician

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.

Job Description:

• As an experienced Biostatistician, you will lead research design and analytical strategies, provide input into protocols, develop and review statistical analysis plans and author/co-author reports, abstracts and manuscripts. You will use your knowledge to advise, provide guidance and to oversee the quality control of statistical deliverables. As the functional lead within a study team, you will direct the Biostatistical activities on a study and be accountable for the deliverables. Senior, Principal, and Senior Principle level Biostatisticians at Parexel are client-facing and play an integral part in the study team.
• Leverage your expertise. Develop complex analysis strategies and execute them using efficient programming techniques (software: SAS, R).
• Foster teamwork. Perform intricate statistical analyses and provide input to statistical reports.
• Share knowledge. Provide input to analysis plans, statistical reports, statistical sections of integrated clinical reports.
• Impact the process. Be a proactive advisor for all types of analysis from the proposal process through the project life cycle.
• Take quality seriously. Review analysis data sets and quality control all types of statistical analysis deliverables.
• Coach and mentor. Train and uplift junior members of the department.

Job Qualifications:

Experience:

• A minimum of 5 years industry (or directly relevant) experience ,A thorough understanding of the statistical aspects of either clinical trials and/or observational studies. Experience in statistical analysis in a clinically related subject, either within clinical trials or in Epidemiology.

SAS programming or R programming skills (desired)

Education:

• A Masters or Ph.D. level education in biostatistics, statistics, mathematics, or another relevant discipline.

Skills:

• Confidence be self-reliant and a quick learner who enjoys working in a matrixed team.
• Good leadership skills.
• Strong oral and written English communication skills.
• The ability to travel as required, although this is not frequent.
• A strong work ethic to promote the development of life changing treatments for patients