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Associate Director, Companion Diagnostics Program Management Precision Medicine

Associate Director, Companion Diagnostics Program Management Precision Medicine

Bristol Myers SquibbMadison, NJ, US
17 days ago
Job type
  • Full-time
Job description

Associate Director, Companion Diagnostics Program Management

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. 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.

Key Responsibilities

In the role as Associate Director, Companion Diagnostics Program Management within Precision Medicine and Translational Science, the ideal candidate :

  • Responsibilities may vary based on project and stages of development (early, late, and lifecycle)
  • Manage the implementation of Biomarker Strategies and Companion Diagnostic projects to support global Development Teams
  • Responsible for managing the Precision Medicine project team and deliverables, working effectively with cross-functional representatives including scientific, clinical, regulatory, legal, finance
  • Responsible for developing and coordinating resource planning across functions to assure that adequate resources are being applied to the project
  • Develop and maintain timelines for Precision Medicine activities, assure alignment with global Development Teams timelines as applicable, update timeline on an ongoing basis to allow transparency to the organization
  • Prepare and track project budgets, manage project financials including accruals and payables, work with Procurement, Business Development, and the Precision Medicine Lead to develop contracts for development partners, service providers, and research collaborators
  • Identify project risks with the project team, develop mitigations and drive for resolution of project issues
  • Prepare regular progress reports and ad hoc reports to facilitate seamless communication and transparency of project status throughout the organization
  • Establish a close partnering relationship with the DT Program Leader and Program Manager, as applicable for the project
  • Establish a close working relationship with external development partners, service providers, and research collaborators to monitor the execution of Precision Medicine projects
  • Ensure that DT strategy recommendations requiring endorsement by governance committees incorporate Precision Medicine team advice, and thoroughly coordinate governance committee planning with the DT
  • Partner with other BMS project management groups and resources to implement project management best practices which facilitate internal efficiencies and information sharing
  • Lead the establishment and harmonization of Precision Medicine related processes, identify needs for process improvements, and lead change management initiatives
  • Assure that BMS values are demonstrated in all aspects of individual actions and team interactions

Basic Qualifications

  • Bachelor's Degree with 12+ years of academic and / or industry experience
  • Or
  • Master's Degree with 10+ years of academic and / or industry experience
  • Or
  • Ph.D. or equivalent advanced degree in the Life Sciences with 8+ years of academic and / or industry experience
  • 4+ years of leadership experience
  • Preferred Qualifications

  • Bachelor's degree with 5-7 years of pharma or medical device experience, 2-3 years project management experience or equivalent; PMP certification desirable.
  • Strong understanding of the global drug development, medical device, and / or translational development processes, with ability to lead supportive project management processes
  • Strong project management skills, outcomes oriented, and results driven
  • Demonstrates effective communication skills, cross-functional collaboration skills, and a cross-cultural awareness
  • Works with independence to effectively lead global, cross-functional matrixed teams.
  • Ability to effectively manage conflicts and negotiations, and influence outcomes without direct authority
  • Excellent organizational, analytical, and planning skills
  • Strong understanding of the project financial budgeting and expenditures process, and contracts development process
  • Effectively utilize project management tools and information technology systems such as Microsoft Office, Teams, Project, Excel, SharePoint, Visio, Spotfire, etc
  • #LI-HYBRID
  • 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.

    Compensation Overview : Cambridge Crossing : $180,430 - $218,638 Madison - Giralda - NJ - US : $156,890 - $190,117. The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit careers.bms.com / life-at-bms / . Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following : Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility / infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program.

    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 a supportive culture, promoting global participation 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 an 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.

    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 / .

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