Hiring.Camp

Associate Director, Drug Development Project Manager

Bristol Myers Squibb

·

Today

Salary
$157k – $190k
Location
Princeton, NJ,US, US
Type
Full-time
Department
IT
Seniority
Entry
Experience
10+ years
Education
PhD
Source
Eightfold

Description

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

Partners with the Global Program Lead (GPL) and Global Project Manager (GPM) to co-lead the strategic and operational planning and decision-making process with a BMS Global Program Team (GPT) in early and/or late development. The Associate Director PM will provide content expertise to the timing, costs, and resources required for development programs and be able to successfully deliver their program(s) milestones and goals. As the strategic partner and operational lead for development and lifecycle management programs, the Associate Director GPM works to ensure that cross-functional teams operate effectively, fostering positive team dynamics and championing BMS’ operating model.

Duties/Responsibilities

  • * The PM partners closely with the Global Program Lead (GPL) and Global Project Manager (GPMT) to lead sub-teams of the Global Program Team (GPT) to drive the development of integrated, efficient, and cross-functional program execution plans.
  • Coordinates and plans the activities for the GPT, including milestone setting, budget forecasting, resource planning, scenario planning, and developing an integrated program plan based on cross-functional inputs and assumptions.
  • Facilitates team goal setting and tracking to ensure adherence to plan and strategy and in preparation for end of year team evaluation process.
  • Manages all associated GPT sub-teams and tracking integrated deliverables and preparing the GPT for governance interactions at program inflection points.
  • The PM is accountable for integrated cross-functional planning bringing together diverse functional plans and strategies, definition of the program operational strategy, management of timelines, budget, quality, and risk assessment and mitigation.
  • The PM works independently to provide best in class operations and project management expertise to drive the GPT and sub-teams toward execution excellence. The PM provides an independent voice to shape the overall project strategy and drive optimal decisions for the broader portfolio value.
  • At the associate director level, the Project Manager (PM) is accountable for one or more GPTs and associates sub-teams of moderate complexity in the early/late development space and is expected to be autonomous in their day-to-day work. The Project Manager may also serve as part of a PM team supporting workstreams of a large, highly complex late stage GPTs with oversight of a Senior PM.
  • Accountable for creating and maintaining a cross-function development plan, timeline and budget for each program and ensuring progress vs. plan.
  • Facilitates effective, science-based business decisions including the generation of multiple development scenarios/options as needed, highlighting interdependencies and downstream impacts (including but not limited to timelines and budget) of strategic decisions.
  • Proactively identifies risks and ensures mitigation plans are implemented.
  • Accountable for communication to team and stakeholders in a transparent and timely manner
  • With the GPL, works to foster a high performing team and monitor the health and operating efficiency of the team as a unit. Leads creation of team norms and operating principles with a focus on cross-functional input and accountability.
  • Develops and coordinates resource and budget planning across functions to assure adequate resources are applied to the project and any changes are highlighted appropriately.
  • Advises on governance expectations and prepares for key decision point discussions with focus on cross-functional input and rigorous debate.
  • For projects that are being jointly developed, works closely with a key strategic alliance partner.
  • Coaches project team members and PM colleagues to drive excellence, accountability, and develops talent pipeline for GPT membership.
  • Change Agent for continuous improvement and transformational initiatives within PM function.
  • Reporting Relationship
  • Reports into a PM Portfolio Lead (Group Lead) or Director, Program Management
  • Qualifications
  • Advanced degree (Ph.D. desirable) in Life Sciences, Chemical Sciences, Physical Sciences, or other relevant discipline. In addition, PMP certification is desirable. BS/MS degrees in a scientific discipline in combination with 8+ years of drug development experience will be considered.
  • The ideal candidate will have 10+ years of experience in biotech/pharmaceutical/health care industry; experience in project/portfolio management or leadership of cross-functional matrix teams is a plus.
  • Proven track record of planning and managing complex programs in early and/or late phase drug development with solid understanding of disease area and drug development pathway with the ability to facilitate and contribute to strategic discussions.
  • Expert understanding of the end-to-end processes in drug development and product value assessment.
  • Leadership skills including situational leadership, ability to lead a team of experts and influence without authority.
  • Demonstrated ability to lead matrix teams, knows how to work at the strategic level with the GPL and when to delve deeper to resolve issues and challenges.
  • Experience with commonly used project management tools including but not limited to Microsoft project.
  • Strong communicator able to integrate and succinctly summarize the various parts of a project and effectively tailor messages to audience including senior leaders.
  • Guides GPT and manages preparation of high-quality documents and presentations for review at governance committees.
  • Ensures appropriate GPT membership during the progression of the program.
  • Ability to resolve complex problems and manage difficult stakeholder situations.
  • Ability to lead the development of critical path analyses and scenario planning.
  • Excellent Project Management Skills – drives execution while balancing speed, quality, and cost.
  • Excellent written and verbal skills, (including full professional English proficiency).
  • Must be well-organized and have strong attention to detail with an ability to deal with competing priorities; high level of problem-solving capability and business acumen, ability to balance competing priorities and quickly and objectively drive the team towards a path which maximizes value, while maintaining the end-to-end cross-functional view.

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: $156,890 - $190,117

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/

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] 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.

R1606652 : Associate Director, Drug Development Project Manager

Skills

Project ManagementProgram ManagementPMP

Similar Jobs

30

Associate Director, Drug Development Project Manager

Bristolmyerssquibb·Princeton Pike - NJ, US

Today

Senior Scientist / Associate Director, Drug Product Manufacturing

BridgeBio Pharma·San Francisco - 1800 Owens·Hybrid, Onsite

Today

Associate Director, Drug Substance, Pulmovant

Pulmovant·Remote, US +1·Remote

5d ago

Associate Director, Drug Safety

Iambic Therapeutics·Remote - US +1·Remote

2w ago

Associate Director, Drug Substance Process Development

Seaport Therapeutics·Boston, MA +1·Onsite

2w ago

Associate Director, Drug Product Development & Manufacturing

Entrada Therapeutics·Boston, MA +1

3w ago

Associate Director, Drug Substance

Celldex·Hampton, NJ

3w ago

Associate Director, Drug Product Development

Mirum Pharmaceuticals·Foster City +1

1mo ago

Senior Manager/Associate Director, Drug Substance MSAT

Ushub Fujifilm·Holly Springs, NC

1mo ago

Senior Manager/Associate Director, Drug Substance MSAT

Us Fujifilm·Holly Springs, NC

1mo ago

Associate Director, Drug Product

Relaytherapeutics·Cambridge, MA

1mo ago

Associate Director, Drug Substance Manufacturing – Upstream Process

"Vera Therapeutics, Inc."·Brisbane, CA +1·Hybrid

1mo ago

Associate Director Drug Product Technical Operations

Vor Bio·Boston, MA +1

2mo ago

Associate Director, Drug Development Excellence

Bristol Myers Squibb·Princeton, NJ +1

2mo ago

Associate Director, Drug Development Excellence

Bristolmyerssquibb·Princeton Pike - NJ, US +1

2mo ago

Associate Director, Drug-Device Combination Development Lead (DDL)

Takeda is an industry·USA - MA - Lexington, US

4mo ago

Associate Director, Drug Product

Cgoncologycareers·Remote·Remote

5mo ago

Mfg Operations Associate Director - Biologics, Drug Substance

vrtx·5000 - Vertex US - Fan Pier, US

1mo ago

Associate Director/Director Drug Product, CMC

Dianthustherapeutics·Remote·Remote

2mo ago

Associate Director/Director Drug Product and Formulation Development

Merida Biosciences·Cambridge, MA

4mo ago

Sr. Manager / Associate Director, Late-Phase Drug Substance PD/MSAT

Merida Biosciences·Cambridge, MA

1mo ago

Associate Director, Technical Operations - Drug Product

Travere Therapeutics·San Diego, US +1·Remote

2mo ago

Associate Medical Director, Global Drug Safety

Astrazeneca·Canada - Mississauga

3mo ago

Associate Medical Director, Global Drug Safety

AstraZeneca·Mississauga, ON

3mo ago

Associate Engineering Director, Combination Drug Product/Device

Neurocrine·US CA San Diego, US·Onsite

3mo ago

Associate Director, Formulation and Drug Product Development

Dynetherapeutics·Waltham, MA +1·Remote, Onsite

5mo ago

Associate Director, Global Project Management- Drug Development

Kyowakirinusa90·Princeton, New Jersey +1

1mo ago

Associate Director of Sales – EMEA (Drug Product Services)

Lonza·FR - Colmar - REMOTE, France +7·Remote

2mo ago

Associate Director, Translational Medicine Lead, Antibody-Drug Conjugates

AstraZeneca is·US – Boston International Place – MA, US

6d ago

Associate Director, Translational Medicine Lead, Antibody-Drug Conjugates

AstraZeneca·Boston, MA

6d ago