Director Program Management at Bristol-Myers Squibb

San Diego, California, United States

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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

Program Management

Cross-Functional Leadership

Drug Development

Regulatory Processes

Risk Management

Clinical Development

Timeline Management

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.

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