Bristol Myers Squibb

Pharmaceutical

Director,BiostatisticsHematology

$217–262k United States FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Director candidates.

The Brief

“Director, Biostatistics Hematology at Bristol Myers Squibb. Skills: Biostatistics, Clinical Trial Design, Statistical Analysis, Drug Development. Drives innovative and efficient study design. Develops study designs that address study objectives”

What You'll Achieve.

support regulatory approval and market access; high quality and timely deliverables; quality of deliverable

Industry & Context.

Pharmaceutical
Problems you'll solve

solve complex statistical problems

Eligibility Requirements

site-essential, site-by-design, field-based, remote-by-design, ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function

What They're Looking For.

Must Have

PhD (9+ years experience) or MS (11+ years experience) in statistics or biostatistics or related scientific field, clinical trials, drug development, pharmaceutical industry or healthcare experience, Proficiency in scientific computing/programming (SAS, R or Python), implementation of advanced statistical analysis, data manipulation, graphing & simulation, Excellent interpersonal, communication, writing and organizational skills, expertise in applying knowledge of general and cutting edge statistical / clinical trials methodology, solve complex statistical problems in the clinical development area, alignment with regulatory agencies and industry standards, Experience in preparing and participating in global regulatory agency interactions, excellent collaboration, organizational/ leadership abilities, and interpersonal skills, development of approaches to enhance the Workforce Planning and Talent Management strategy of the internal and external talent pools within a therapeutic area

Nice to Have

at least 3 years management (direct or matrix) experience is preferred

What You'll Do.

Drives innovative and efficient study design

Develops study designs that address study objectives

support regulatory approval

medical research and market access

and oversees statistical support

Provides guidance and management to statisticians

ensure high quality and timely deliverables

Contributes to Clinical Development Plans

leads GBDS related submission activities

post-submission strategies/ preparations/defenses

Provides statistical support and leadership

address health authority request

and other public release of information

Compliant with BMS processes and SOPs

adherence to global and project standards

responsible for quality of deliverable

Contributes to creation/maintenance of and provide training on statistical topics departmental SOPs

Manages a functional or project budget

allocate company resources according to project needs

ensure consistency and adherence to standards

Represents BMS at professional societies

industry-wide technical discussions

Contributes to the statistical community of practice

Provides active coaching to biostatistical team members

develops solutions to problems

Effectively communicates the GBDS Mission and Vision

excitement and commitment within GBDS

Enables a culture of inclusiveness

respect for diversity

compliance with process

allows for the questioning and challenging of others

Provides leadership to empower and develop the team

Provides guidance to employee's development plans

carries out performance review and feedback

Develops performance metrics for staff

How You'll Work.

Team & Collaboration

member of cross-functional team; Engages as a matrix team member on high level development teams; act as a scientific and strategic partner in the drug development process; Presents and defends complex statistical solutions to all levels of BMS governance, key stakeholders and external regulatory bodies; Provides guidance and management to statisticians; Provides active coaching to biostatistical team members; Effectively engages as an employee advocate and management coach/mentor to team members both internally and externally; Provides leadership to empower and develop the team

Communication Scope

communication; writing; organizational skills; interpersonal skills

Process & Methodology

Manages a functional or project budget, allocate company resources according to project needs, set priorities, ensure consistency and adherence to standards

Full Job Description

**Working with Us** Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. 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. Read more: [careers.bms.com/working-with-us](https://careers.bms.com/working-with-us). At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, cell therapy, immunology, cardiovascular and neuroscience 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. **Position Summary** Director of Biostatistics is a member of cross-functional team and contributes to development of compounds within a therapeutic area. Drives the design of innovative and efficient clinical trials, including the selection of populations to study and endpoints to use. Develops trial designs that address study objectives that will support regulatory approval and market access. Contributes to Clinical Development Plans, submissions, and post-submission strategies, preparations, and defenses. Provides guidance and management to statisticians to ensure high quality and time

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