Associate Director, US Medical Promotional Review Scientist, Neuroscience

Position Summary

The Associate Director, US Medical Promotional Review Scientist - Neuroscience, plays a critical role in the Medical Communications team within Global Medical Affairs. As a member of this team, you will serve as a strategic, solutions-oriented partner focused on ensuring the medical accuracy and scientific validity of promotional and non-promotional materials, across Neuroscience brands and disease areas.

This includes ensuring robust scientific evidence and compliance with US laws and regulations. This role reports to the Director, Medical Promotional Review, Neuroscience (Medical Communications) within Global Medical Affairs.

Key Responsibilities

The Associate Director, Medical Promotional Review Scientist is accountable for the following:

• Maintain therapeutic area and product knowledge through ongoing assessment of relevant neuroscience published literature, treatment guidelines, internal resources, and data
• Provide strong medical guidance in interdisciplinary meetings and related initiatives, including promotional review, disease/brand and launch planning, labeling changes, and business reviews
• As a member of the Medical Promotional Review (PReP) Advisor team, conduct reviews of promotional, non-promotional, and proactive materials for scientific and medical validity, as well as adherence to BMS SOPs
• Critically evaluate and offer strategically sound solutions for complex promotional and non-promotional tactics to ensure message balance, key clinical findings, medical accuracy, robust support, and content appropriateness in accordance with relevant guidelines (e.g., clinical guidelines, FDA/OPDP guidance)
• Proactively align and build strong relationships with marketing, access, medical, corporate communications, training, legal, and commercial regulatory affairs to ensure consistent messaging across stakeholders
• Demonstrate leadership within the medical review team to drive best practices aligned with strategic imperatives, currency on changing regulations, and Commercial strategy; participate in initiatives aimed at process improvements related to core medical activities
• Provide medical advice and guidance on draft product labeling to ensure commercially viable US labeling for future promotion and advertising
• Participate in internal and external meetings (e.g., training, education, medical congresses, and matrix team meetings) to stay current on regulations, medical/scientific developments, and Commercial and Medical strategy
• Review and evaluate evidence supporting promotional claims to ensure they are comprehensive, balanced, unbiased, and statistically reliable, while advising stakeholders on appropriate scientific interpretation
• Apply digital and AI-driven solutions to improve efficiency, consistency, and scalability of promotional review activities
• Stay informed of industry trends and promote best practice sharing across medical and promotional review teams
• Complete all assigned SOPs and training within designated timeframes and adhere to job-specific SOPs and work instructions
• Conduct business in accordance with BMS Values
• Serve as an exceptional individual contributor and foster a high-performing, externally focused culture that promotes teamwork, collaboration, personal accountability, and a commitment to quality; model and reinforce BMS behaviors at all organizational levels

Qualifications & Experience

• Advanced scientific degree (PharmD, PhD, or MD preferred)
• Minimum of 3-5 years of direct pharmaceutical/healthcare industry experience within Promotional Review; therapeutic area experience preferred
• Thorough understanding of medical writing and promotional material review in the pharmaceutical industry
• Proven ability to manage multiple projects, solve problems, deliver on commitments, and work with multidisciplinary teams
• Strong scientific/medical written and verbal communication skills
• Knowledge of the pharmaceutical industry and external compliance, transparency, and conflict-of-interest environments
• Experience delivering customer-focused service
• Flexibility in response to changing needs and competing demands
• Developed business acumen and ability to influence senior internal stakeholders
• Strong team player with individual initiative, a positive attitude, and accountability
• Strong leadership and organizational skills with demonstrated success in driving optimal business results in a complex matrix organization
• Strategic leadership, performance management, alignment building, negotiation, and collaboration skills
• Proven ability to work in an ambiguous environment
• Experience working on teams through change and navigating complex organizational dynamics.
• Ability to analyze and interpret trial data; significant experience with FDAMA 114 content, Real World Evidence, and other data consistent with FDA-approved labeling (CFL)
• Strong stakeholder relationship-building and negotiation skills
• Ability to travel 10-25% (domestically and internationally)

• #LI-HYBRID
• 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.

Compensation Overview

Princeton - NJ - US: $155,540 - $188,480

The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully - carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.

Benefits

Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans - including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability).

• U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year.
• Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays.

Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day.

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.

Data Protection

• We will never request payments, financial information, or social security numbers during our application or recruitment process.
• Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

• If this posting is missing required information required by local law or incorrect, contact BMS at with the Job Title and Requisition number.
• Do not send application-related inquiries to this email.
• To check your application status, please login to your Candidate Home Account.

R1607814: Associate Director, US Medical Promotional Review Scientist, Neuroscience