Principal Statistician

  • Anywhere

Company :
Bristol-Myers Squibb

Location :
Princeton, New Jersey

Expiry Date :
Mon, 14 Dec 2020 23:59:59 GMT

Apply Job :
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Description :
At Bristol Myers Squibb, we are inspired by a single vision transforming patients lives through 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. Responsibilities will include, but are not limited to, the following: – Actively provide statistical support to the Clinical R & D Department. – Provide statistical input into the design of protocols including preparation of the biostatistical analysis section. Suggest optimal statistical designs that are acceptable by regulators. – Prepare statistical analysis plans including table shells. – Analyze and report results of clinical trials. Provide tables, listings and graphs for final study reports. Provide ad hoc/data driven analyses. – Provide statistical input for the preparation of final study reports and other required documents. – Provide statistical support for integrated reports, submissions preparation, and post- submission activities. – Contribute to Clinical Development Plan. – Support preparation of manuscripts. – Provide project requirements to programmers. – Serve as statistical lead on studies, projects, NDAs or sNDAs. – Represent the company in interfaces with regulatory agencies globally. – Provide statistical input to senior management. – Manage outside CROs and consultants as needed. – Work closely with different departments in the company (regulatory, clinical, marketing, data management, health economics, etc.) and provide statistical support for a variety of functional groups. – Provides leadership – Sought out statistical expert to peers and others – Provides supportive feedback to peers and leaders – Proactively seeks ways to gain broader experience/perspectives and make contributions – Participates in cross-functional collaboration and meetings to gain the trust and respect of members, make decisions on business issues and freely challenges and expresses opinions – May provide coaching and mentoring and provides feedback via formal/informal appraisals Skills/Knowledge Required: – Ph.D. or MS in statistics with a focus on statistical methods appropriate for clinical trials. – Experience in clinical drug development of at least 5 years for Ph.D. and 7 years for MS. – Good planning and project management skills with experience in a pharmaceutical statistical department including direct interaction with clinical personnel. – Demonstrated skill in the planning, analysis and reporting of clinical trials. . – Detailed knowledge of statistical regulatory requirements/regulations and currently acceptable statistical methodologies. – Excellent SAS skills.. Willingness to be hands-on when needed. – Knowledge of MS Office products (Word, Excel, PowerPoint) – Good interpersonal, communication, writing and organizational skills. – Demonstrated ability to work in a team environment with medical personnel, clinical monitors, data managers, programmers and medical writers. 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.