Associate Director, Veeva Clinical Engineering & Operations
Company: Disability Solutions
Location: Princeton
Posted on: October 19, 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:
.Position Summary: Accountable for implementing and supporting
strategic information systems that enable Global Development
Operations (GDO) function, specifically focusing on Veeva Clinical
Vault (Veeva CTMS, Veeva eTMF). This role owns end-to-end
responsibility for managing the build and run of GDD technology
assets, ensuring they are reliable, accessible, & secure. Specific
responsibilities:
- Partner with IT Product Managers to plan, prioritize, deliver &
support strategic digital capabilities and ensure maximum value is
achieved.
- Identify, design, and develop technical solutions to meet
business demand.
- Manage the build and run of technology assets.
- Manage Total Cost of Ownership (build & run) and the key
drivers behind them to ensure the digital capabilities are cost
efficient.
- Influence vendor roadmaps to align with BMS strategy.
Requirements:
- Must have 10+ years of related work experience in a
Biopharmaceutical environment.
- BS/BA in Engineering, Computer Science or Life Sciences (or
other quantitative related discipline). Graduate Degree or
higher-level education preferred.
- Must have Veeva Clinical Vault expertise, with specific
knowledge of Veeva CTMS and eTMF.
- Must have broad technology expertise, strong working knowledge
of Pharmaceutical R&D business processes, particularly in
Clinical Trial Operations, with demonstrated command of key
concepts, systems and processes.
- Preferred - certified in Veeva Vault Administration
- Should have a demonstrated track record in implementing complex
technical solutions, developing software applications following
structured SDLC processes in a regulated (GxP) environment and
leading technical teams.
- Demonstrated competency in execution of multiple large projects
simultaneously within a Product Model leveraging Agile methods,
from concept initiation through delivery and steady-state
operations.
- Experience working with offshore software development models is
preferred.
- Critical thinking in dealing with complex technical issues and
working with key business stakeholders to develop solutions for
short-term remediation and long-term strategy.
- Experience in evaluating new technologies, delivery methods
(e.g., SaaS/PaaS/IaaS), and services, and influencing the
negotiation process for vendor products.
- Must possess excellent written and verbal skills and
demonstrate an ability to effectively communicate at all levels of
the organization including executive stakeholders.
- Ability to achieve successful consensus among differing
priorities and stakeholders in both the IT and Business
communities.
- Must be a relationship builder and capable of working
effectively in a highly matrix organization with strong
communication, planning, and collaboration skills. 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 . Visit 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.If
you live in or expect to work from Los Angeles County if hired for
this position, please visit this page for important additional
information: Any data processed in connection with role
applications will be treated in accordance with applicable data
privacy policies and regulations.
Keywords: Disability Solutions, Union , Associate Director, Veeva Clinical Engineering & Operations, Executive , Princeton, New Jersey
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