Sr Director, RWE Biostatistics
Company: Disability Solutions
Location: Madison
Posted on: May 3, 2024
Job Description:
Working with UsChallenging. 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 rich in diversity. 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 .At Bristol Myers Squibb, we are
inspired by a single vision - transforming patients' lives through
science. In oncology, hematology, cell therapy, immunology,
Neuroscience, 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.Position Summary The Senior
Director of Real-World Evidence Biostatistics plays a pivotal role
in leading and overseeing the strategic direction and execution of
statistical and real-world evidence initiatives within the
organization. This key leadership position involves providing
guidance and expertise in statistical methodologies, study design
using real-world data to facilitate and support development and
regulatory interactions of pharmaceutical products. The Senior
Director collaborates closely with cross-functional teams to drive
innovation, optimize trial design, and leverage real-world data to
support evidence generation and decision-making. Additionally, the
role involves representing the organization in interactions with
regulatory agencies, fostering a culture of excellence and
continuous improvement within the Global Biometrics and Data
Sciences, and serving as a thought leader in the field of
real-world evidence.Key Responsibilities
- Provide strategic leadership in the design, execution, and
analysis of real-world evidence studies
- Lead efforts to enhance the utilization of real-world data for
evidence generation and decision-making purposes
- Represent the organization at conferences, forums, and industry
events to showcase expertise and thought leadership in
biostatistics and real-world data
- Manages resources and budget to ensure company resources are
allocated according to the development needs and priorities
- Creates effective processes related to RWE and ensures
consistency and adherence across therapeutic areas and
projects
- Key contributor to Clinical Development Plans, submissions, and
post-submission strategies/preparation/ defense as needed
- Represents the company in interfaces with regulatory agencies
globally
- Effectively engages as a matrix team member on high-level
development teams and serves as a scientific and strategic
partner
- Seeks and establishes new collaborations with cross-functional
teams for RWE objectives
- 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
- 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 staffQualifications & Experience
- PhD or MS (12+ 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
- Extensive experience in real-world data within the
pharmaceutical or CRO industry, demonstrating a strong track record
of leadership and strategic thinking.
- In-depth knowledge of statistical methodologies, clinical trial
design, and real-world evidence generation, with a focus on
optimizing study design and data analysis
- A commitment to continuous learning and professional
development in the field of real-world data
- Experience in preparing and participating in global regulatory
agency interactions
- Demonstrate excellent collaboration, organizational/ leadership
abilities, and interpersonal skills
- At least 5 years management (direct or matrix) experience is
preferred If you come across a role that intrigues you but doesn't
perfectly line up with your resume, we encourage you to apply
anyway. You could be one step away from work that will transform
your life and career. Uniquely Interesting Work, Life-changing
CareersWith a single vision as inspiring as Transforming patients'
lives through science--- , every BMS employee plays an integral
role in work that goes far beyond ordinary. Each of us is empowered
to apply our individual talents and unique perspectives in an
inclusive culture, promoting diversity in clinical trials, while
our shared values of passion, innovation, urgency, accountability,
inclusion and integrity bring out the highest potential of each of
our colleagues.On-site Protocol BMS has a diverse occupancy
structure that determines where an employee is required to conduct
their work. This structure includes site-essential, site-by-design,
field-based and remote-by-design jobs. The occupancy type that you
are assigned is determined by the nature and responsibilities of
your 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 these roles, onsite presence is considered an
essential job function and is critical to collaboration,
innovation, productivity, and a positive Company culture. 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. BMS is dedicated to ensuring that people with
disabilities can excel through a transparent recruitment process,
reasonable workplace accommodations/adjustments and ongoing support
in their roles. Applicants can request a reasonable workplace
accommodation/adjustment prior to accepting a job offer. If you
require reasonable accommodations/adjustments in completing this
application, or in any part of the recruitment process, direct your
inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/
eeo -accessibility to access our complete Equal Employment
Opportunity statement. BMS cares about your well-being and the
well-being of our staff, customers, patients, and communities. As a
result, the Company strongly recommends that all employees be fully
vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
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, Jersey City , Sr Director, RWE Biostatistics, Executive , Madison, New Jersey
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