Senior Director, Early Clinical Development (MD) - Neuroscience

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”, a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

Job Description

The Senior Director, Global Clinical Development, Neuroscience will own the clinical strategy for one or more neuropsychiatry programs. Extensive experience in clinical development in neuropsychiatric indications is a requirement. Experience in formulation development in neuropsychiatry is a plus.

The Neuroscience Clinical Development function is part of a global scientific organization dedicated to initial evaluations of new molecules, biomarkers, and mechanistic hypotheses in humans. The group drives clinical strategy, and the design, execution, and interpretation of studies to select the most promising drug candidates for development.

Position Summary / Objective

Serve as the clinical point of accountability for the Clinical Development Team and responsible for the overall clinical development plan for asset(s) in one or more indication(s)

Demonstrate matrix leadership to develop, motivate and achieve results through teamwork

Ensure studies are designed to meet Regulatory, Quality, medical, and access goals

Position Responsibilities

Medical Monitoring

Serves as a Clinical Trial Physician for clinical trials by Developing and implementing the clinical development strategy

Analyzing, interpreting, and leveraging clinical trial data towards further clinical development

Serving as principal functional author for Regulatory submissions, Clinical Study Reports, and scientific publications

Independently synthesizes and/or contributes to plans (e.g., trial design, development strategy, regulatory strategy) based on emerging data and input from relevant functions

Designs and develops clinical studies and research plans in support of asset strategy with the program and clinical development teams

  Clinical Development Expertise & Strategy

Manages multiple/complex programs concurrently across clinical lifecycles

Accountable for clinical contribution to the development of indication strategy

Partners with Worldwide Patient Safety physicians in the ongoing review and interpretation of safety data

Provides clinical leadership and disease area expertise into integrated disease area strategies

Partners closely with KOLs in specific indications

Evaluates strategic options against a given Target Product Profile (TPP)

Collaborates with Global Development Operations/Global Compliance Group to develop asset level risk management plan, resolves issues with Quality/Clinical Scientists, and brings it to the Clinical Development Team as needed

Sets executional priorities and partners with Clinical Scientists and Clinical Trial Physicians to support executional delivery of studies

Accountable for top line data with support of Clinical Scientists and Statisticians

Liaises with Clinical Scientists, Translational & Discovery Scientists, and Development Teams to define dose and schedule, indications, and patient selection (e.g., biomarker qualification and implementation)

Ad-Hoc involvement in various departmental or enterprise initiatives (e.g., committees, sub-teams etc.)

Presents and/or articulates clinical strategy to senior leadership and to support progression of portfolio

Health Authority Interactions

Serves as primary clinical representative in regulatory interactions

Accountable for clinical contributions to clinical study reports (CSRs), regulatory reports, briefing books and submission documents

External Partnerships, Alliances, and Publications

Acts as a focal point for defining and establishing relationships with key investigators

Sits in team responsible for establishing key alliances with academic centers, co-operative groups, vendors and government agencies

Represents department in business development due diligence and partner alliance management as appropriate; sits on JDC/JRC/JSC as appropriate

Leadership and Matrix Management

May be responsible for managing Clinical Trial Physicians and Clinical Scientists, attracting, developing and retaining top talent; ensures appropriate training and mentoring of other physicians and scientists

Champions a quality-focused mindset and ensures adherence to GCP and compliance obligations for clinical conduct

Degree Requirements

MD or MD/PhD and deep clinical development expertise in psychiatry

Fellowship/specialty training in relevant therapeutic area preferred

Experience Requirements

7+ years of relevant experience in translational and/or clinical research in an industry or biotech setting

Extensive experience in clinical trial design and execution, and development strategy in pharmaceutical industry or biotech

Deep understanding of pharmaceutical discovery, development and commercialization

Track record of mentorship and/or management and/or matrix leadership

Demonstrated leadership abilities in a matrix environment

Travel Required

Domestic and International travel may be required

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

How We Work

Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working .

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to  adastaffingsupport@bms.com . Visit  careers.bms.com/eeo-accessibility  to access our complete Equal Employment Opportunity statement.

Bristol Myers Squibb is Disability Confident – Employer

A UK Government scheme

Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

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R1608135 : Senior Director, Early Clinical Development (MD) - Neuroscience