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  1. Home
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  5. Senior Director, Global Clinical Development, Neuroscience
Bristol Myers Squibb logo

Senior Director, Global Clinical Development, Neuroscience

Not Disclosed•Full-TimeOn-site

location_onPeabody Street, Neighborhood Nine, Cambridge, Middlesex County, Massachusetts, 02318, United States

Apply Now

Working with Us

Challenging, meaningful, and life-changing work happens every day at Bristol Myers Squibb. From optimizing production lines to driving breakthroughs in cell therapy, our teams transform the lives of patients while advancing their own careers. We recognize the importance of balance and flexibility, offering a wide variety of competitive benefits and programs to support our employees in pursuing their goals both at work and in their personal lives.

With a vision to "Transform patients' lives through science," every employee plays an integral role in work that goes far beyond the ordinary. Our shared values of passion, innovation, urgency, accountability, inclusion, and integrity bring out the highest potential of our colleagues, empowering individuals to apply their unique talents in a supportive culture that promotes global participation in clinical trials.

About the Role

The Clinical Development Lead sits within Clinical Development, a global organization dedicated to the effective design and execution of drug development. This role serves as the clinical point of accountability for the Development Team, responsible for the overall clinical development plan for assets in one or more indications or tumor types. As a matrix leader, you will lead, develop, and motivate teams to achieve results, ensuring studies are aligned with target label indications and designed to meet regulatory, quality, medical, and access goals.

You will partner with Clinical Trial Physicians (CTPs) and Clinical Scientists to drive the clinical contribution to indication strategies, including registrational and non-registrational studies. This position requires a commitment to developing a resilient attitude, embracing change, and championing a quality-focused mindset to ensure adherence to Good Clinical Practice (GCP) and compliance obligations. You will represent Clinical Development in internal and external forums as the consulted authority for the disease area, collaborating with Key Opinion Leaders (KOLs) and serving as the primary clinical representative in regulatory interactions.

Hiring Process & Application

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.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process. Applicants can request reasonable workplace accommodations or adjustments prior to accepting a job offer. If you require accommodations during the application or recruitment process, please direct your inquiries to adastaffingsupport@bms.com.

Equal Opportunity & Culture

Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.

We consider qualified applicants with arrest and conviction records pursuant to applicable laws. For candidates in Los Angeles County, additional information regarding employment rights is available on our careers site. We will never request payments, financial information, or social security numbers during our application or recruitment process.

Work location

Work model: On-site

location_on

Peabody Street, Neighborhood Nine, Cambridge, Middlesex County, Massachusetts, 02318, United States

Cambridge, Massachusetts

Key Responsibilities

  • check_circleRepresent Clinical Development in regulatory interactions and external forums as a disease area authority
  • check_circlePartner with Key Opinion Leaders to align clinical strategies with disease area treatment paradigms
  • check_circleLead clinical development strategy and execution for drug assets across one or more indications
  • check_circleCollaborate with Global Development Operations to develop and resolve asset-level risk management plans
  • check_circleManage, develop, and mentor Clinical Trial Physicians to ensure team excellence
  • check_circleOversee clinical content for regulatory reports, briefing books, and submission documents
  • check_circleDesign, execute, and analyze clinical studies in partnership with Clinical Scientists
  • check_circleEnsure adherence to GCP, quality standards, and compliance obligations for clinical conduct

Requirements

  • verifiedMD required
  • verifiedAt least 10 years of relevant experience
  • verifiedDeep understanding of clinical principles
  • verifiedExperience as Clinical Trial Physician, Clinical Scientist, or equivalent
  • verifiedVerifiable track record of successful people management
  • verifiedExperience leading matrix teams
  • verifiedAbility to design and execute multiple clinical trials
  • verifiedKnowledge of GCP and compliance obligations
  • verifiedExperience with regulatory submission documents
  • verifiedAbility to synthesize internal and external data for clinical strategy
  • verifiedExperience with early, late, and post-marketing development

Benefits & Perks

check_circleMedical, pharmacy, dental, and vision care coveragecheck_circle401(k) plan with financial well-being and protection optionscheck_circleShort- and long-term disability, life insurance, and accident insurancecheck_circleEmployee Assistance Programs (EAP) and BMS Well-Being AccountFlexible time off (unlimited) with 11 paid national holidays for US Exempt Employees
Bristol Myers Squibb logo
Company

Bristol Myers Squibb

Industry

scientific & qa

View company profilearrow_forwardlanguageWebsite
Quick Overview

Experience

10+ yrs (Lead)

Education

MD required with deep understanding of clinical principles

Job Type

Full-Time

Skills Required

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Skills, education and keywords

Skills: Clinical Development Strategy, Clinical Trials, GCP, Regulatory Submission, Phase Ii-Iii Trials, First In Human, Proof Of Concept Trials, Target Product Profile, Risk Management Plan, Clinical Trial Physician.

Education: MD required with deep understanding of clinical principles.

Frequently asked questions about Senior Director, Global Clinical Development, Neuroscience at Bristol Myers Squibb

What does a Senior Director, Global Clinical Development, Neuroscience at Bristol Myers Squibb do?expand_more
A Senior Director, Global Clinical Development, Neuroscience at Bristol Myers Squibb is responsible for the following: Represent Clinical Development in regulatory interactions and external forums as a disease area authority; Partner with Key Opinion Leaders to align clinical strategies with disease area treatment paradigms; Lead clinical development strategy and execution for drug assets across one or more indications; and Collaborate with Global Development Operations to develop and resolve asset-level risk management plans.
What are the requirements for this Senior Director, Global Clinical Development, Neuroscience role?expand_more
Bristol Myers Squibb is looking for candidates who meet the following requirements: MD required; At least 10 years of relevant experience; Deep understanding of clinical principles; Experience as Clinical Trial Physician, Clinical Scientist, or equivalent; Verifiable track record of successful people management; and Experience leading matrix teams.
Where is the Senior Director, Global Clinical Development, Neuroscience role at Bristol Myers Squibb located?expand_more
Senior Director, Global Clinical Development, Neuroscience at Bristol Myers Squibb is based in Peabody Street, Neighborhood Nine, Cambridge, Middlesex County, Massachusetts, 02318, United States. This is a on-site role.
Is this Senior Director, Global Clinical Development, Neuroscience job remote, hybrid, or on-site?expand_more
Bristol Myers Squibb has listed this Senior Director, Global Clinical Development, Neuroscience role as on-site.
How much experience is required for this Senior Director, Global Clinical Development, Neuroscience role?expand_more
Senior Director, Global Clinical Development, Neuroscience at Bristol Myers Squibb typically requires 10+ years of relevant experience at the lead level.
What skills do you need for the Senior Director, Global Clinical Development, Neuroscience role at Bristol Myers Squibb?expand_more
Key skills for Senior Director, Global Clinical Development, Neuroscience at Bristol Myers Squibb include Clinical Development Strategy; Clinical Trials; GCP; Regulatory Submission; Phase Ii-Iii Trials; First In Human; Proof Of Concept Trials; and Target Product Profile.
What education is required for Senior Director, Global Clinical Development, Neuroscience at Bristol Myers Squibb?expand_more
Educational requirements for this role: MD required with deep understanding of clinical principles.
What category does the Senior Director, Global Clinical Development, Neuroscience role belong to?expand_more
Senior Director, Global Clinical Development, Neuroscience at Bristol Myers Squibb is part of the scientific & qa job category on Recrutus.
Recrutus

Curating the world's most innovative career opportunities. We bridge the gap between visionary talent and industry-leading companies.

Search roles by city, category, skill, or job type — explore verified US employers, salary benchmarks, and remote-friendly teams hiring nationwide.

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Recrutus helps candidates discover roles that match their skills and helps teams reach qualified applicants faster. Browse by metro, discipline, or work style — from internships to senior leadership.

© 2026 Recrutus. All rights reserved.
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verified
Ability to build relationships with external partners and thought leaders
check_circle
check_circle160 hours annual paid vacation for Phoenix, AZ, Puerto Rico, and Rayzebio Exempt/Non-Exempt/Hourly Employees
check_circleUp to 2 paid volunteer days per year and unlimited paid sick time
check_circleLeaves of absence for medical, personal, parental, caregiver, bereavement, and military needs
check_circleAnnual Global Shutdown between Christmas and New Years Day for eligible global employees
check_circleSummer hours flexibility for eligible US office-based employees
Clinical Development StrategyClinical TrialsGCPRegulatory SubmissionPhase Ii-Iii TrialsFirst In HumanProof Of Concept TrialsTarget Product ProfileRisk Management PlanClinical Trial Physician
US privacy notice
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