Associate Director, Project Management, Clinical Data Ecosystem, GDD IT - Bristol Myers Squibb
Princeton, NJ
About the Job
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 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.
Working at BMS:
At BMS, digital innovation and Information Technology are central to our vision of transforming patients’ lives through science. To accelerate our ability to serve patients around the world, we must unleash the power of technology. We are committed to being at the forefront of transforming the way medicine is made and delivered by harnessing the power of computer and data science, artificial intelligence, and other technologies to promote scientific discovery, faster decision making, and enhanced patient care.If you want an exciting and rewarding career that is meaningful, consider joining our diverse team!
Position Summary:
We areseekinga highly motivated and detail-orientedAssociateDirector -ProductManagerwith broad clinical data experienceto join our IT team within the Clinical Data Ecosystem team. The successful candidate will play a critical role in supporting the development, implementation, and optimization of competitive trial design, intelligence and optimization solutionsand collaborate across functions to deliver value.This position offers an exciting opportunity to work at the intersection of technology and clinical research, contributing to the advancement of innovative therapies and improving patient outcomes.
The successful candidate willbe responsible fordefining the product strategy, roadmap, and execution plan to enhance our clinical data management capabilities. This role requires a deep understanding of clinical data processes, strong leadership skills, and the ability to drive cross-functional collaboration.TheProduct Managerwill work closely with globalclinical, biometrics and data sciencestakeholders, includingdata scientists,software developers, project managers, andcross functionalIT teams, to ensure successfulstrategy, planning,delivery,and operations of technology solutionsto accelerate bringing effective therapies and drug to patients andlong-termvalue toBMS.
Key Responsibilities:
Product Development and Management:
Develop and communicate a clear product vision and strategy for the clinical data ecosystemespecially withclinical trial design and data science methodologies to enable clinical data exploration.
Create and maintaina product roadmap that aligns with businessobjectivesand stakeholder needs.
Prioritize features and enhancements based on user feedback, and business value
Lead the end-to-end product development lifecycle, from ideation to launch and post-launch optimization.
Collaborate with cross-functional teams, including clinical operations, data management, IT, and external vendors, to deliver high-quality products.
Define and track key performance indicators (KPIs) to measure product success and drive continuous improvement.
Data Analysis and Reporting:
Develop andmaintaindashboards, reports, and visualizations to support data-driven decision-making.
Ensure data integrity and accuracy across all clinical data systems.
StakeholderEngagement:
Act as the primary point of contact for stakeholders, ensuring clear communication and alignment on product goals and priorities.
Gather and analyze feedback from users and stakeholders to inform product decisions and enhancements.
Provide regular updates to senior leadership on product status, risks, and opportunities.
Qualifications & Experience:
Master's or bachelor'sdegree in computer science, Information Technology, Life Sciences, or a related field.
6-8years of experience in a product manageror similar role within the pharmaceutical or biotechnology industry.
Excellent analytical, problem-solving, and communication skills.
A self-starterand the ability to work independently and as part of a team in a fast-paced, dynamic environment.
Prior experience working in an Agile/Product based environment.
Strong understanding of clinical data systems (e.g., EDC, CTMS, CDMS, CDM, CDR, SCE).
Proficiency in data analysis tools and languages (e.g., SQL, Python, R) and data visualization tools (e.g., Tableau, Power BI).
Proficiency inmachine learning models,exposure tolarge language models and generative AI technologieswill be necessary for the role.
Hands on AI imaging and deep learning experience is a plus
Knowledge of regulatory requirements and industry standards (e.g., GCP, CDISC) is a plus.
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 Careers
With 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 toadastaffingsupport@bms.com. Visitcareers.bms.com/eeo-accessibilityto 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: https://careers.bms.com/california-residents/
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
