Principal Biostatistician Lead - FSP

Parexel, USA - Any Region - Home Based

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Date Posted September 01, 2020
Industry Private Sector BioStat Jobs
Specialty Not Specified
Job Status Not Specified
Salary Not Specified

Description:

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.

Responsibilities

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 expertise to advise, provide guidance and to oversee the quality control of statistical deliverables. As the functional lead within a study team, you will lead the Biostatistical activities on a study and be accountable for the deliverables. Senior and Principal level Biostatistician at Parexel are client-facing and play an integral part in the study team.

Our Biostatistics teams are not only focused on delivering quality results for our client’s needs, but also value working with one another in a flexible environment. Although some team members are home-based and others are office-based, our virtual resources support our teams to work collaboratively and effectively across the globe.

Around 30% of our Biostatistics team have been a part of the Parexel family for a minimum of 5 years. Our team is made up of experienced and highly educated professionals in our field. This is truly a statistic that speaks for itself!


In this role you may:

Supervise, advise and review:
Lead and cooperate:

Qualifications

Education:
  • PhD or Masters (with sufficient work experience) in a statistical discipline required

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 skills required, R programming skills a plus

Skills:
  • Confident, self-reliant and a quick learner who enjoys working in a matrix team
  • Good leadership skills
  • Strong oral and written English communication skills
  • Ability to travel as required, although this is not frequent
  • Work ethically and honestly to promote the development of life changing treatments for patients

EEO Disclaimer

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.
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