Bristol Myers Squibb
AssociateDirector,Biostatistics
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“Associate Director, Biostatistics at Bristol Myers Squibb. Skills: Biostatistics, statistical analysis, clinical trials methodology. Collaborates in design of innovative and efficient clinical trials, including the selection of study population/endpoints to address study objectives, and contributes to project development strategy. Defends protocols and analysis plans at internal governance reviews and provides independent reviews of complex protocols.”
What You'll Achieve.
address study objectives; quality of deliverable
Industry & Context.
advanced statistical analysis; data manipulation; graphing; simulation
On-site Protocol: Site-essential, Site-by-design, Field-based and Remote-by-design jobs. Occupancy type determined by nature and responsibilities of the role., Site-essential roles require 100% of shifts onsite at your assigned facility., Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility., For field-based and remote-by-design roles the 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 (6+ years’ experience) or MS (8+ years’ experience) in statistics or biostatistics or related scientific field with clinical trials, drug development, pharmaceutical industry or healthcare experience, Proficiency in scientific computing/programming (SAS, R or Python) and implementation of advanced statistical analysis, data manipulation, graphing & simulation., Great interpersonal, communication, writing and organizational skills, Expertise in statistical/clinical trials methodology as it related to clinical development and ability to apply to relevant clinical development framework, Good understanding of regulatory landscape and experience with participating in regulatory interactions., Demonstrate collaboration, organizational/ leadership abilities, and interpersonal skills, Demonstrate ability to plan, organize, and prioritize multiple work assignments, and project management skills
Nice to Have
People manager experience is preferred (for people manager position only)
What You'll Do.
Collaborates in design of innovative and efficient clinical trials
including the selection of study population/endpoints to address study objectives
and contributes to project development strategy
Defends protocols and analysis plans at internal governance reviews and provides independent reviews of complex protocols.
Independently authors and/or reviews protocol
statistical analysis plan
clinical study reports
associated publications
and other study level documents
Presents summary data and analyses results
and transparent manner.
Provides statistical support and leadership to address health authority request
and other public release of information
Manages multiple studies to ensure consistency and adherence to standards within an indication or therapeutic area.
Applies extensive knowledge of statistical / clinical trials methodology as it relates to clinical development.
Invests in developing knowledge outside of traditional statistical expertise in the clinical
regulatory and commercial environments with demonstrated application to study design.
Effectively engages as a matrix team member on project teams
to act as a scientific and strategic partner in the drug development process.
Compliant with BMS processes and SOPs
adherence to global and project standards within an indication or therapeutic area and responsible for quality of deliverable.
Contributes to external and internal statistical community of practice
Develops & advises team members
Effectively communicates the GBDS Mission and Vision in a fashion that generates pride
excitement and commitment within GBDS.
Enables a culture of inclusiveness
respect for diversity
compliance with process and allows for the questioning and challenging of others in a respectful and constructive manner.
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.
Provides guidance to employee's development plans and carries out performance review and feedback.
develops performance metrics for staff.
How You'll Work.
Team & Collaboration
Effectively engages as a matrix team member on project teams, to act as a scientific and strategic partner in the drug development process.; Develops & advises 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
Great communication skills; writing skills; Presents summary data and analyses results, in a clear, concise, complete, and transparent manner.; Effectively communicates the GBDS Mission and Vision in a fashion that generates pride, excitement and commitment within GBDS.
Process & Methodology
Demonstrate ability to plan, organize, and prioritize multiple work assignments, project management skills
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). **_Key Responsibilities_** ·Collaborates in design of innovative and efficient clinical trials, including the selection of study population/endpoints to address study objectives, and contributes to project development strategy ·Defends protocols and analysis plans at internal governance reviews and provides independent reviews of complex protocols. ·Independently authors and/or reviews protocol, statistical analysis plan, clinical study reports, associated publications, and other study level documents ·Presents summary data and analyses results, in a clear, concise, complete, and transparent manner. ·Provides statistical support and leadership to address health authority request, publication, presentation, and other public release of information ·Manages multiple studies to ensure consistency and adherence to standards within an indication or therapeutic area. ·Applies extensive knowledge of statistical / clinical trials methodology as it relates to clinical development. ·Invests in developing knowledge outside of tradition
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