Bristol Myers Squibb Company

Senior Statistician

Location
Celgene, NJ, United States
Posted
Sep 03, 2020
Ref
R1529312
Required Education
Doctorate/PHD/MD
Position Type
Full time
At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

About Bristol-Myers Squibb

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

Responsibilities will include, but are not limited to, the following:

Actively provide statistical support to the Clinical R&D Department.
  • Contribute to efficient study design, prepare statistical consideration sections and provide input into other protocol sections.
  • Prepare statistical analysis plans including table shells.
  • Analyze clinical trial data; work with programmers to provide tables, listings and graphs, including ad hoc validation.
  • Review, synthesize, interpret and report analysis results.
  • Provide ad hoc data driven analyses.
  • Provide statistical input for the preparation of final study reports and other required documents.
  • Support preparation of manuscripts.
  • Provide statistical support for integrated reports, submissions preparation, and post-submission activities.
  • Provide project requirements to programmers.
  • Manage outside CROs and consultants as needed.
  • Escalates issues to functional management as necessary.
  • Makes recommendations or resolves technical, quality, and timeline issues.
  • Provides leadership
  • Provides continuous feedback to peers and leaders
  • Proactively seeks ways to gain broader experience/perspectives and focuses on a robust professional development plan


Skills/Knowledge Required:
  • Ph.D or MS. in statistics with a focus on statistical methods appropriate for clinical trials.
  • Experience in clinical drug development at least 2 years for Ph.D and 5 years for MS.
  • Demonstrated skill in the analysis and reporting of clinical trials.
  • Knowledge of statistical methodologies and statistical regulatory requirements.
  • Knowledge of statistical computing software (e.g. SAS or R).
  • Knowledge of MS Office products (Word, Excel, PowerPoint)
  • Strong knowledge of clinical trial design concepts.
  • Knowledge of clinical drug development process.
  • Experience working in a team environment with other clinical team members.\\Good interpersonal, communication, writing and organizational skills.


Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.