Position SummaryWe are searching for a highly motivated Program Manager to support Translational Development Leaders within the Solid Tumor pillar of Translational Development to enable the effective and efficient execution of translational development plans. The Translational Program Manager, as part of the Translational Development team in Research, would manage multiple complex, oncology portfolio assets and facilitate broad, integrated biomarker plans to enable delivery of the Translational Development portfolio across solid tumor indications.
Key Responsibilities:- Provide program management support for Translational Development teams across assigned studies, assets, and disease-area workstreams.
- Partner with Translational Development Leads, biomarker scientists, clinical teams, laboratory teams, data and analytics teams, operations partners, and vendors to translate project objectives into actionable plans, timelines, deliverables, and follow-up actions.
- Coordinate execution of biomarker and translational activities, including assay testing, vendor coordination, data delivery, and documentation of key decisions and outcomes.
- Develop, maintain, and communicate integrated timelines for translational activities, including sample logistics, assay development and testing, data transfers, analyses, reporting milestones, and study deliverables.
- Facilitate cross-functional meetings by preparing agendas, tracking action items, documenting decisions, and ensuring timely completion of commitments.
- Coordinate biospecimen, informed-consent, data-use, and data-transfer activities required to support translational studies and collaborations.
- Support management of external laboratories, vendors, and CROs by tracking contracts, statements of work, deliverables, budgets, invoices, timelines, and issue resolution.
- Monitor project risks, dependencies, and critical-path activities; develop mitigation plans and escalate issues when appropriate.
- Support biomarker budget tracking, forecasting activities, contract management, and purchase-order processes as required.
- Maintain project documentation and collaborative tools, including SharePoint sites, dashboards, trackers, meeting repositories, contact lists, and reporting tools.
- Support publication and congress planning activities through tracking abstracts, timelines, authorship coordination, review milestones, and data-readiness requirements.
- Identify opportunities to improve operational efficiency, consistency, transparency, and communication across translational project activities.
Qualifications & Experience:- B.S. or M.S. in a scientific discipline; project management certification or equivalent project management experience is desirable.
- 5+ years of pharmaceutical, biotechnology, or related industry experience in operational, scientific, translational development, biomarker, or clinical development roles within a matrixed environment.
- Experience coordinating multiple projects involving cross-functional teams, external collaborators, vendors, laboratories, and operational stakeholders.
- Experience supporting translational, biomarker, clinical development, or research programs, including sample management, data generation, vendor oversight, and deliverable tracking.
- Demonstrated ability to manage timelines, priorities, risks, dependencies, and communications across multiple concurrent projects.
- Strong communication, facilitation, and stakeholder engagement skills.
- Experience working with project management, collaboration, visualization, and reporting tools.
#LI-Hybrid
We hire for skills and capabilities, not just credentials - if this role excites you, but doesnt perfectly match your resume, we encourage you to apply anyway.
Compensation Overview:Madison - Giralda - NJ - US: $119,030 - $144,241
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 Years Day.
U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits
How We WorkWhere 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.
