Associate Director, Statistical Programming
Company: Disability Solutions
Location: Princeton
Posted on: September 1, 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 .Project Responsibilities:
- Provides comprehensive programming leadership and support to
complex clinical project teams and vendors, including deployment of
programming strategies, standards, specifications and programmed
analysis to comply with regulatory requirements, SOPs and work
practices
- Drives the development and implementation of innovative
strategies and technologies for clinical trial programming
- Independently develops, validates, troubleshoots, and maintains
complex programs and utilities in accordance with predefined
specifications and standards
- Leads the electronic submission preparation and review
- Develops unambiguous and robust programming specifications
(e.g. ADaM specifications)
- Reviews planning documents (e.g., statistical analysis plan,
data presentation plan, data review plan) to align with project
objectives and ensures clarity and completeness of programming
assumptions and requirements; Assesses document robustness and
impact on programming activitiesImprovement Responsibilities:
- Drives, Identifies, leads, and supports opportunities to
enhance processes and technology
- Communicates proactively and effectively around issues and
risks and contributes to its remediationManagerial
Responsibilities:
- Effectively recruits, manages, develops, evaluates, rewards,
motivates, and retains direct reports, resulting in an increasing
level of capabilities within GBDS
- Conducts objective setting, performance check-ins, and year-end
discussions in compliance with BMS policies; aligns objectives,
feedback and performance evaluation with manager
- Meets regularly with direct reports, focusing on project
updates, development needs, issue resolution, and provides
real-time coaching and feedback; holds staff accountable for
quality and timeliness of programming activities; ensures staff is
compliant with training requirements
- Communicates with manager regarding promotions, performance
concerns, and retention risks
- Builds and maintains a network with stakeholders and peers to
ensure cross-functional strategies and objectives intertwine and
build upon each other to achieve results
- Act as extended member of Statistical Programming Leadership
Team in sharing and building up the line function visionMinimum
Requirements:
- Bachelor's degree in statistics, biostatistics, mathematics,
computer science or life sciences required
- At least 10 years programming experience in industry including
support of significant regulatory filings and minimum 5 years of
experience in managing technical professionals in a regulated
environment
- For US positions: US military experience will be considered
towards industry experience
- Proficient knowledge of drug development process, clinical
trial methodology, regulatory guidance, industry standards,
statistical concepts, and medical terminology used in the analysis
and submission of clinical data
- Broad expertise in statistical programming and in developing
computing strategies
- In-depth understanding of clinical data structure (e.g. CDISC
standards) and relational databases
- Demonstrated proficiency in using SAS to produce analysis
datasets and TFLs and in using other software tools and
applications (e.g. MS office, XML, Pinnacle 21)
- Demonstrated ability in processing of upstream data (e.g.
multiple data forms, workflows, eDC, SDTM); Demonstrated ability in
providing deliverables to meet downstream requirements, (e.g. ADaM,
TFLs, e-submission components)
- Demonstrated ability to work in a team environment with
clinical team membersPreferred Requirements:Member of industry
organizations or presented at Congresses/ConferencesIf 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, Trenton , Associate Director, Statistical Programming, Executive , Princeton, New Jersey
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