Bristol Myers Squibb
Director, Global Clinical Physician, Late Hematology, Oncology, and Cell Therapy (HOCT)
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Director, Global Clinical Physician - Late Hematology, Oncology, and Cell Therapy (HOCT)
Working at Bristol Myers Squibb
Challenging. Meaningful. Life-changing. These are the kind of words that rarely get associated with work—but at Bristol Myers Squibb, nothing is usual. Here, groundbreaking science unfolds every day across every department. Whether you're refining production protocols or advancing revolutionary cell therapy research, your work will shape the lives of patients—and the trajectory of your own career. With opportunities in scale and distinction that defy the ordinary, you'll thrive alongside high-performing teams while personally growing like never before.
Bristol Myers Squibb values balance and flexibility. Explore our competitive suite of benefits, programs and services at careers.bms.com/working-with-us.
Position Summary
This Director, Global Clinical Physician role sits within Late Clinical Development of the Haematology, Oncology, and Cell Therapy (HOCT) department. As a key medical leader, you’ll ensure clinical programs reach their full potential by providing scientific oversight from early/late-phase development through registration.
Your expertise will align supportive medical leadership across cross-functional teams and strategically advance therapies that matter the most. For patients. For BMS.
Key Responsibilities
- No direct reports; leverage matrix influence across the Clinical Development Team (CDT)
- Global medical leadership: Inform strategic clinical development aligned with therapeutic priorities
- Protocol expertise: Input on clinical trial design—protocols, endpoints, eligibility criteria
- Bridging roles: Medical input into safety signals, data interpretation, and risk-benefit assessment
- Cross-functional collaboration: Partner with clinical scientists, regulatory affairs, and stakeholders to ensure high-quality trial execution
- Site interactions: Investigator engagement and medical education activities
- Regulatory significance: Support submissions to health authorities (FDA, EMA, etc.) and companion documents
- Stay ahead: Monitor evolving therapies, competitive landscapes, and scientific innovation
- Conference participation: Represent BMS through international interactions
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Key Requirements
Basic Qualifications
✔ MD or equivalent required ✔ Clinical experience specifically in haematology, oncology, or related fields ✔ Track record in clinical research and drug development ✔ Expertise in GCP adherence, regulatory frameworks, and clinical trial processes ✔ Strong ability to work in matrix structures with collaborative cross-functional teams
Preferred Qualifications
🔹 Fellowship in hematology or oncology 🔹 Experience in late-phase development (Phase 2–3, or registration) 🔹 Prior medical monitoring involvement 🔹 Experience working with FDA/EMA or similar global regulators 🔹 Scientifically distinguished track record (publications, conferences)
Core Competencies
- Strong scientific judgment and medical expertise
- Strategic thinking and analytical problem-solving
- Cross-functional partnership across development teams
- Communication: stakeholder relationships and concise information trust
- Ability to navigate complexity and balance competing priorities
Travel Requirements
Up to ~20–30% of your time will involve domestic and international travel:
- Investigator meeting attendance
- Scientific conference presentations (e.g., ASCO, EHA, BMT) or physician engagement
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Company Culture and expectations
Working principles:
- Transforming lives through science
- Global operations with patient perspectives front and centre
- Flexible and supportive environment
- Bristol Myers Squibb, Disability Confident Employer – Learn more about accessibility
On-Site/Travelling Expectations:
BMS classifies roles according to physical work location requirements—Site-essential, Site-by-design, Field-based, Remote. For this role, ensure eligibility for: ✅ Onsite collaboration (BMS Centres or investigator partner sites) ✅ Attendance at top-tier scientific hubs (investigator, regulatory, or partner visits)
About Disability Support
BMS is committed to accessibility. For reasonable accommodation accommodations at any stage of recruitment, reply to:
- adastaffingsupport@bms.com with disability-related access needs.
At BMS, Adaptability = Opportunity—we develop our role models together.
Contact Queries & Compliance
For EEO formatting questions or discrepancies: TAEnablement@bms.com Apply and track via Chat with Ripley.
For general fraud-prevention: Fraud Alerts. BMS will never request:
- Payment of fees
- Personal/funding details
- Social security numbers or sending money.
Data Protection follows all applicable law with transparency during application processing.
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