Associate Director, Biostatistics
Company: Disability Solutions
Location: Princeton
Posted on: October 19, 2024
Job Description:
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. Purpose The Associate
Director, Biostatistics is a core member of cross-functional
development teams and contributes to trial design, protocol
development, analysis planning, interpretation of results,
preparation of regulatory submissions and publications.
Statisticians develop collaborative relationships and work
effectively with the Global Biometric Sciences (GBS) Lead, the GBS
Planning and Execution Lead, statistical programmers, external
partners, medical monitor, protocol manager, data manager, PK
scientist, and other members of the study/indication team. Primary
Responsibilities
- Core member of an EDT and key sub-teams. Contributes to all
aspects of the development strategy.
- Independently leads the development and execution of
statistical aspects for one or more clinical trials, including
contribution to study trial design, analysis planning, study
results presentation and interpretation, clinical study report
authoring, regulatory submissions and publications.
- Participates in development strategy, protocols and analysis
plans reviews.
- Participates in continuous improvement initiatives.
- Invests in knowledge outside of traditional statistical
expertise in the clinical, regulatory and commercial environments
that impact the development teams.
- Engages as a matrix team member on protocol teams as a
scientific partner in the drug development process.
- Ability to present summary data and analyses to key
stakeholders in a clear, concise, complete and transparent
manner.
- Possesses technical knowledge of statistical methodology and
ability to appropriately apply it in trial design and data analysis
for clear, concise, high-quality results.
- Takes accountability for ensuring quality in all planning,
design and execution of assignments associated with the assigned
protocol or project. Education/Experience
- PhD degree in Statistics or Biostatistics or Master's degree
with 7+ years' of relevant Pharmaceutical/R&D or other related
experience, including supporting regulatory filings.
- Demonstrated knowledge of statistical / clinical trials
methodology as it relates to clinical development.
- Relevant prior data analysis planning, execution and delivery
experience.
- Excellent verbal and written communications skills.
- Ability to be flexible and adapt quickly to the changing needs
of the organization.
- strong interpersonal skills evidenced in interactions with
individuals at all levels of the organization, and demonstrated
ability to develop relationships within the organization and
leverage the formal and informal organizational structure to assist
in goal achievement, including the resolution of conflicts or their
appropriate escalationAround 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.
Physical presence at the BMS worksite or physical presence in the
field is an essential job function of this role which the Company
deems critical to collaboration, innovation, productivity, employee
well-being and engagement, and enhances the Company culture.To
protect the safety of our workforce, customers, patients and
communities, the policy of the Company requires all employees and
workers in the U.S. and Puerto Rico to be fully vaccinated against
COVID-19, unless they have received an exception based on an
approved request for a medical or religious reasonable
accommodation. Therefore, all BMS applicants seeking a role located
in the U.S. and Puerto Rico must confirm that they have already
received or are willing to receive the full COVID-19 vaccination by
their start date as a qualification of the role and condition of
employment. This requirement is subject to state and local law
restrictions and may not be applicable to employees working in
certain jurisdictions such as Montana. This requirement is also
subject to discussions with collective bargaining representatives
in the U.S.Our company is committed to ensuring that people with
disabilities can excel through a transparent recruitment process,
reasonable workplace adjustments and ongoing support in their
roles. Applicants can request an approval of accommodation prior to
accepting a job offer. If you require reasonable accommodation in
completing this application or if you are applying to a role based
in the U.S. or Puerto Rico and you believe that you are unable to
receive a COVID-19 vaccine due to a medical condition or sincerely
held religious belief, during or any part of the recruitment
process, please direct your inquiries to . Visitto access our
complete Equal Employment Opportunity statement.BMS will consider
for employment qualified applicants with arrest and conviction
records, pursuant to applicable laws in your area. Any data
processed in connection with role applications will be treated in
accordance with applicable data privacy policies and
regulations.
Keywords: Disability Solutions, Passaic , Associate Director, Biostatistics, Executive , Princeton, New Jersey
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