Director Program Management at Bristol-Myers Squibb

San Diego, California, United States

Apply Now

Not SpecifiedCompensation

Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level

Full TimeJob Type

UnknownVisa

Biotechnology, Pharmaceuticals, RadiopharmaceuticalsIndustries

Requirements

Advanced degree (PhD, PharmD, MD, or MBA) in Life Sciences, Medicine, or related discipline
Minimum 10 years’ experience in drug development and program management within the pharmaceutical/biotech industry
Direct leadership experience of cross-functional teams and complex R&D programs
Demonstrated track record of successfully delivering early-stage programs through regulatory submissions across different geographies
Clinical-stage program management expertise
Deep understanding of drug development and regulatory processes across different geographies
Ability to assess and drive deployment of tools and best practices to ensure successful product development

Responsibilities

Partners with Program Team Lead to drive cross-functional program teams
Partners with functional leaders (Research, Regulatory, CMC, Clinical Development, etc.) to align on program strategy and drive execution in line with corporate objectives
Develops, refines, and manages complex program timelines; pressure-tests plans and creates alternative scenarios to address risks and dependencies
Proactively identifies risks and challenges; implements effective mitigation strategies, and communicates risks and solutions to program and leadership
Facilitates productive team meetings, develops agendas, and documents decisions and action items to ensure accountability and progress
Communicates effectively with team members and stakeholders, fostering an environment of collaboration, transparency, and high performance
Challenges assumptions, timelines and expenses at the program level; pressure tests plans; and creates alternative scenarios, highlighting interdependencies and downstream impacts of strategic decisions
Provides leadership to team members, challenging conventional thinking to approach problems differently, with faster execution and elevated outcomes
Acts as a program management subject matter expert, understands best practices, identifies gaps and challenges, implements efficiencies and improved ways of working within the organization
Contributes to the development of junior program managers

Skills

Key technologies and capabilities for this role

Program ManagementCross-Functional LeadershipDrug DevelopmentRegulatory ProcessesRisk ManagementClinical DevelopmentTimeline Management

Questions & Answers

Common questions about this position

What benefits does Bristol Myers Squibb offer?

Bristol Myers Squibb offers a wide variety of competitive benefits, services, and programs that provide employees with resources to pursue their goals both at work and in their personal lives.

Is this position remote or based in a specific location?

The company is headquartered in San Diego, CA, but specific location or remote work details for this role are not specified.

What skills and experience are required for the Senior Director of Program Management role?

The role requires clinical-stage program management expertise, deep understanding of drug development and regulatory processes across geographies, and the ability to assess and drive deployment of tools and best practices.

What is the company culture like at Bristol Myers Squibb and RayzeBio?

The culture emphasizes challenging, meaningful, life-changing work in a flexible environment with high-achieving teams, collaboration, transparency, and high performance.

What makes a strong candidate for this Director Program Management position?

A strong candidate has experience leading cross-functional teams in clinical-stage drug development, expertise in managing complex timelines and risks, and the ability to partner with functional leaders to drive program strategy and execution.

Bristol-Myers Squibb

Develops and delivers biopharmaceutical medicines

About Bristol-Myers Squibb

Bristol Myers Squibb (BMS) develops and delivers medicines aimed at treating serious diseases, focusing on areas like cancer, autoimmune diseases, and heart conditions. The company conducts extensive research and development to create new drugs, which are sold after receiving regulatory approval. BMS also produces generic drugs, offering affordable alternatives that meet the same quality standards as their branded counterparts. What sets BMS apart from competitors is its dual focus on both innovative and generic medicines, enhancing access to healthcare. The company's goal is to improve patient outcomes while maintaining a commitment to sustainability and corporate responsibility.

New York City, New YorkHeadquarters

1887Year Founded

$33,706.1MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees

Benefits

Flexible Work Hours

Hybrid Work Options

Professional Development Budget

Risks

Increased competition in oncology from emerging biotech firms like ArsenalBio.

BMS's lawsuit over the 340B Drug Pricing Program may lead to regulatory challenges.

Rapid AI and digital tech evolution may pose integration challenges for BMS.

Differentiation

BMS focuses on innovative cancer treatments through collaborations like ArsenalBio for T cell therapies.

The company emphasizes digital health technologies, enhancing clinical trial management and patient engagement.

BMS offers both innovative and generic medicines, increasing affordable healthcare solutions.

Upsides

BMS's partnership with Medidata enhances clinical research processes and patient outcomes.

The collaboration with AI Proteins advances novel miniprotein-based therapeutics, expanding therapeutic modalities.

BMS's global license agreement with BioArctic expands its portfolio in neurodegenerative diseases.

Land your dream remote job 3x faster with AI

Try Jobo Free