Director, MEG Lead Hematology, Medical Evidence Generation at Bristol-Myers Squibb

Princeton, New Jersey, United States

Bristol-Myers Squibb Logo
Not SpecifiedCompensation
Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceuticals, BiotechnologyIndustries

Requirements

  • Advanced scientific degree (MD, PhD, or PharmD or the equivalent) required with extensive, relevant scientific, and/or clinical experience
  • At least 7 years of experience in pharmaceutical clinical development, Medical Affairs or relevant Commercial experience; previous customer-facing role experience highly desirable
  • Demonstrated ability to strategically analyze data generation opportunities with minimal supervision
  • Demonstrated ability to develop and sustain high-performing relationships with external thought leaders and internal matrix stakeholders
  • Adeptness at building credibility with external investigators and collaborative partners competently balancing business and scientific acumen complemented by strong leadership behaviors, authenticity, agility, and an enterprise mindset
  • Understanding of global healthcare systems and academic settings with a demonstrated ability to lead in ambiguous and changing healthcare/business environments
  • Exceptional communication and interpersonal skills to influence decision-making at all levels of the organization
  • In depth knowledge of overall project planning and project management of clinical trials
  • Proven ability to partner effectively with colleagues across multiple functions and at all levels of the enterprise

Responsibilities

  • Facilitate collaborative exchange between BMS and thought leaders in community practice and academia, including scientific dialogue and representing BMS as a trusted, inclusive, and innovative industry collaborator and partner of choice
  • Be accountable for delivering CRCs, ISRs, and MASTs from concept ideation to governance approval and throughout the study lifecycle
  • Act as point of contact for CRCs, ISRs, and MASTs within Therapeutic and Disease area teams
  • Design and drive strategies to accelerate the development of BMS’s clinical development pipeline leveraging external research platforms, technologies, and insights
  • Align with and advise senior functional and therapeutic area leaders on new external opportunities that will inform strategy and influence decisions in the creation/refinement of integrated evidence generation plans
  • Personally lead a limited number of high-visibility projects leveraging relevant disease subject matter expertise
  • Contribute to the evolution of MEG therapeutic area strategy and value proposition

Skills

Key technologies and capabilities for this role

HematologyMedical Evidence GenerationClinical Research CollaborationsInvestigator-Sponsored ResearchMedical Affairs Sponsored StudiesThought Leader EngagementStudy Lifecycle ManagementScientific DialogueEvidence Gap AnalysisPipeline Development

Questions & Answers

Common questions about this position

What qualifications are required for the Director, MEG Lead Hematology role?

An advanced scientific degree such as MD, PhD, or PharmD (or equivalent) is required, along with at least 7 years of experience in pharmaceutical clinical development, Medical Affairs, or relevant Commercial experience, and extensive relevant scientific and/or clinical experience.

Is this position remote or does it require working from an office?

The position is based at the Lawrenceville (PPK) or Madison (GIR) site in New Jersey.

What is the salary for this role?

This information is not specified in the job description.

What is the company culture like at Bristol Myers Squibb?

BMS offers a challenging, meaningful, and life-changing work environment with uniquely interesting work every day, opportunities to grow and thrive alongside high-achieving teams, and a focus on balance and flexibility.

What experience makes a strong candidate for this position?

Candidates with an advanced scientific degree, at least 7 years in pharmaceutical clinical development, Medical Affairs, or Commercial roles, previous customer-facing experience, and expertise in hematology or evidence generation will stand out.

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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