Senior Vice President, Global Development Operations at Bristol-Myers Squibb

Princeton, New Jersey, United States

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Not SpecifiedCompensation

Expert & Leadership (9+ years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceutical, BiotechnologyIndustries

Requirements

Bachelor's degree in Science or Business, Advanced degree strongly preferred
Significant experience (20+ years) of drug development or related experience managing clinical and CMC development under a variety of contexts; multiple clinical trials and operations required (ideally with pharma co and/or CRO)
A demonstrated track record of success leading, engaging, managing, and developing a large global multi-site, multi-cultural organization
Leadership experience of a large-scale enterprise transformation at global level, with a significant R&D component as a key driver (renewal of portfolio, development cycle, M&A activity)
Ability to develop strong working relationships with key internal stakeholders and outside of BMS (functional and project leaders, peers and employees at all levels, vendors, Pharma industry community)

Responsibilities

Member of the Drug Development Leadership Team, reporting to the Chief Medical Officer
Anticipates & drives strategic evolution of GDO function and provides strong leadership and vision for the function and in the execution of clinical trials
Manages, builds and leads global development operations function to execute and achieve functional responsibilities and program goals in compliance with GCP, ICH and other global regulatory requirements
Provides comprehensive strategic leadership for 2,100+ multi-site organization across 40+ countries; including Regional Clinical Operations, Global Trial Management, Global Data Management and Trial Delivery Support
Optimizes clinical trial costs, CRO contracts as part of continued strategic value capture
Accountable to deliver innovative digital solutions to optimize and accelerate the clinical trial process
Collaborates with development heads to establish clear strategy & objectives for clinical trials and programs including estimation and articulation of risks/benefits
Delivers on BMS Diversity Commitments by increasing patient voice and diversity in BMS-conducted clinical trials
Maintains full GCP compliance and ensures the highest ethical standards of clinical trial and business conduct
Ensures that all operations comply with local HR, health, safety, environmental/risk management legislation and GCP as well as with corporate compliance policies
Identifies and grows the next generation of GDO and DD leaders in partnership with the rest of the DD Leadership Team
Influences beyond area of responsibilities to drive innovation agenda by partnering with all relevant stakeholder groups incl. Research, GPS, Commercialization and supporting functions
Maintains global leadership and external reputation that attracts outstanding staff and commands respect of investigators to provide competitive superiority for BMS

Skills

Key technologies and capabilities for this role

Clinical OperationsGCPICHGlobal Trial ManagementData ManagementCRO ManagementRegulatory ComplianceStrategic LeadershipTeam Leadership

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 a remote position or does it require office work?

This information is not specified in the job description.

What is the salary for the Senior Vice President role?

This information is not specified in the job description.

What leadership experience is required for this role?

The role requires strong leadership and vision for a global function, managing a 2,100+ multi-site organization across 40+ countries, including Regional Clinical Operations, Global Trial Management, Global Data Management, and Trial Delivery Support.

What makes a strong candidate for this position?

A strong candidate will have experience leading global clinical operations, driving strategic evolution, ensuring GCP compliance, optimizing trial costs and digital solutions, and growing future leaders within a large-scale organization.

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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