Associate Statistical Project Leader

Job Title: Associate Statistical Project Leader

Location: Morristown, NJ Cambridge, MA

About the Job

Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress. Join our Biostatistics Neurology team as Associate Statistical Project Leader and you’ll l ead one or several late phase studies, or lead an indication for a complex compound, under supervision of statistical project leader and/or team leader.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Main Responsibilities

• Provide high quality input into the design of the clinical study, the setup and conduct of the study

• Accountable for all statistical deliverables related to the study

• Oversee execution of the statistical analyses according to the statistical analysis plan: perform and/or coordinate with study programmer the production of statistical analyses

• Prepare statistical methods & provide statistical insight into interpretation and discussion of results sections for the clinical study report and/or publications to ensure the statistical integrity of the content according to internal standards and regulatory guidelines

• Propose, prepare and perform exploratory data analyses, ad-hoc analyses as relevant for the study or project objectives

• Provide technical guidance to junior staff

• Plan and track study activities and timelines

• Ensure productive collaborations with other functions in the aligned study team, promoting teamwork, operational efficiency, and innovation

• Represent statistics to participate in scientific or technology working groups or cross function initiatives.

About You

Education and Experience :

• PhD in Statistics or related discipline with at least 3 years of pharmaceutical experience in clinical development, including late phase

• MS in Statistics or related discipline with at least 5 years of pharmaceutical experience in clinical development, including late phase

​Technical skills :

• Broad knowledge and good understanding of advanced statistical concepts and techniques; able to do advanced statistical analyses using SAS or R

Soft skills :

• Demonstrated strong interpersonal and communication skills

Languages :

• Proficient in written and spoken English

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Why Choose Us?

• Bring the miracles of science to life alongside a supportive, future-focused team.

• Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.

• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.

• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.

All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

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All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.