Bristol Myers Squibb

Bristol Myers Squibb

Posted via Workday

Associate Director, Alliance Management - eCOA

Apply by May 31, 2027

Posted Oct 29, 2026

Role at a glance

Salary
Not yet verified Check the description for pay details; an amount or pay period has not been verified.
Location
Princeton, New Jersey, United States
Employment
Full-time
Experience
A minimum of 5-7 years industry experience (pharma, biotech, CRO) required
Education
Bachelor’s degree or relevant experience

Spotted an issue?

We’ll check it against the original posting.

Log in to report

Role Summary

AI-generated

The Associate Director, Alliance Management - eCOA manages existing business partnerships with preferred eCOA vendors in alignment with the needs of key internal BMS stakeholders. The role provides end-to-end oversight of eCOA services across neuroscience clinical programs, including vendor performance oversight, risk management, and issue resolution.

What You'll Do

  • Coordinate with the partner counterpart on overall portfolio delivery, including timely execution of the book of work under the MSA and...
  • Provide end-to-end oversight of eCOA services across neuroscience clinical programs, from vendor selection and study start-up through...
  • Co-lead governance meetings, including Operational and Strategic Management Committees and other project meetings as needed.
  • Liaise with internal clinical teams, regional colleagues, subject matter experts, and partner stakeholders to identify and resolve...
  • Drive collaborative continuous improvement initiatives and communication and training to ensure adherence to the operating model.
  • Collaborate with the BMS quality organization and the partner to drive effective quality management of outsourced trials.

Generated from the employer's posting. Verify important details before applying.

View full posting

Qualifications

Bachelor’s degree or relevant experience with 5-7 years of pharma, biotech, or CRO industry experience, including neuroscience and eCOA expertise.

Required

  • Bachelor’s degree or relevant experience
  • A minimum of 5-7 years industry experience (pharma, biotech, CRO) required
  • Neuroscience clinical development experience, including understanding of neuroscience study designs, patient populations, endpoints and...
  • Deep, hands-on experience managing eCOA end to end across the clinical trial lifecycle, including strategy, licensing, implementation,...
  • Strong Project Management and Stakeholder Management skills
  • First-hand experience of working directly with Contract Service Providers (CSPs), investigators, customers, opinion leaders and...
  • Demonstrated ability to effectively communicate to a diverse audience at multiple levels within the company
  • Demonstrated ability of managing and working with cross-functional / global cross-country people/teams in a complex, changing environment

Preferred

  • Ability to review contracts and negotiate contracts
  • Scientific, financial, and business problem-solving experience

Original job description

Content provided by the employer

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.



Position Summary

 

The Associate Director, Alliance Management is responsible for managing existing business partnerships with preferred electronic Clinical Outcome Assessment (eCOA) vendors in alignment with the needs of key internal BMS stakeholders. The role requires deep, hands-on experience managing eCOA services across the full clinical development lifecycle—from strategy, study design and instrument implementation through deployment, data delivery, closeout and vendor performance oversight—with particular expertise supporting neuroscience clinical development programs. Success requires clear communication of BMS expectations, objective measurement of vendor performance, proactive management of operational and compliance risks, and efficient resolution of service delivery deviations so BMS teams can continue the critical work of helping patients prevail over serious diseases

Key Responsibilities

 

  • Coordinate with partner counterpart with focus on overall portfolio delivery including ensuring timely execution of the book of work while adhering to the MSA and Quality Agreement.
  • Provide end-to-end oversight of eCOA services across neuroscience clinical programs, including vendor strategy and selection, study start-up, instrument licensing and implementation, system configuration and validation, site and patient deployment, data quality and delivery, change control, issue escalation, closeout and lessons learned.
  • Co-lead and drive efficient and effective governance meetings, including Operational and Strategic Management Committees and additional project meetings as necessary.
  • Liaise with internal clinical teams, regional colleagues, key subject matter experts and stakeholders in other functions and within partner’s organization to embed the operational model, and to identify and resolve issues and gaps.
  • Drive collaborative continuous improvement initiatives with the partner to streamline and improve operational processes.
  • Drive communication and training to ensure adherence to the operating model and efficient execution.
  • Collaborate with the BMS quality organization and partner to drive effective quality management of outsourced trials.
  • Support MSA/partnership contract negotiations as necessary
  • Collaborate with other BMS business units that outsource clinical trials to ensure alignment of information, best practices, and to standardize processes were applicable.
  • Provide outsourcing perspective and ensure proactive consideration of impact to outsourced studies, for BMS processes and requirements, and facilitate change management with partner for associated process revisions.
  • Ensure proper communication to development organization and stakeholders regarding outsourcing strategies and activities.

 

Qualifications & Experience


  • Bachelor’s degree or relevant experience
  • A minimum of 5-7 years industry experience (pharma, biotech, CRO) required; scientific, financial, and business problem-solving experience desired
  • Neuroscience clinical development experience required, including a strong understanding of neuroscience study designs, patient populations, endpoints and operational complexities.
  • Deep, hands-on experience managing eCOA end to end across the clinical trial lifecycle, including eCOA strategy, instrument and language licensing, implementation, configuration and validation, integrations, site and patient enablement, data delivery and reconciliation, change control, issue and risk management, vendor governance, and study closeout is required.
  • Strong Project Management and Stakeholder Management skills
  • Ability to review contracts and negotiate contracts preferred
  • First-hand experience of working directly with Contract Service Providers (CSPs), investigators, customers, opinion leaders and professional staff as well as broad exposure to the pharmaceutical industry
  • Demonstrated ability to effectively communicate to a diverse audience at multiple levels within the company
  • Demonstrated ability of managing and working with cross-functional / global cross-country people/teams in a complex, changing environment

#LI-hybrid


We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

Compensation Overview:

Princeton - NJ - US: $170,640 - $206,773

The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully – carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.


Benefits:


Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans – including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability).


U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year.


Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays.


Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day.


U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits


How We Work

Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.


Supporting People with Disabilities

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 [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.


Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.


For roles based in Los Angeles County only:  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/


For roles based in Washington State only: If you live in or expect to work from Washington State if hired for this position, please visit this page for important information about the Washington Fair Chance Act.


Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.


Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.


If this posting is missing required information required by local law or incorrect, contact BMS at [email protected]with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.



R1607673 : Associate Director, Alliance Management - eCOA
Bristol Myers Squibb

About the company

Bristol Myers Squibb

Large Enterprise

Bristol Myers Squibb is a global biopharmaceutical company committed to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. With a focus on oncology, immunology, and cardiovascular health, the company leverages advanced science and technology to create transformative therapies that address critical unmet medical needs. Operating in more than 70 countries, Bristol Myers Squibb emphasizes collaborative efforts and strong partnerships in research and development to drive advancements in healthcare and improve patient outcomes worldwide.