E.R. Squibb & Sons,L.L.C. Posted November 11, 2026

Senior Manager, REMS Advisor Lead

Field, United States Full time
Medical Affairs Manager
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E.R. Squibb & Sons,L.L.C. is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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.

The REMS Advisor Lead is responsible for building, developing, and leading a high-performing team of REMS Advisors who deliver exceptional REMS program education to certified prescribers and healthcare professionals. This role drives operational excellence by optimizing the prescriber and patient experience, collaborating with cross-functional BMS teams, and overseeing the development of REMS processes, materials, and technologies. We seek a dynamic leader who inspires their team to deliver superior service, fosters a culture of continuous improvement, and ensures REMS education is delivered with clarity, empathy, and impact.

Responsibilities include, but are not limited to the following:

REMS Advisor Team Leadership & Development

Partner with the Director, REMS Advisors to develop and execute operational strategies for daily team management, scalability planning, and geographic expansion

Assess current team structure and forecast future operational needs to ensure the REMS Advisor Team can scale effectively based on program demands and geographic distribution

Lead the full employee lifecycle for REMS Advisors, including recruitment, hiring, onboarding, performance management, coaching, and development planning

Collaborate with the Director, REMS Advisors and Learning & Development Team to design and implement comprehensive, ongoing training curricula for REMS Advisors

Direct all training activities in partnership with the REMS Training Team, ensuring REMS Advisors demonstrate required competencies before performing their roles independently

Ensure REMS Advisor staff maintains compliance with all REMS program training and mandatory corporate training requirements

Coach and mentor REMS Advisors to achieve performance excellence; establish Individual Development Plans (IDPs) that align short- and long-term career aspirations with business needs

Guide goal-setting processes using SMART criteria to establish clear, measurable departmental and individual objectives

Continuously monitor staffing levels and workload capacity; develop business justification documentation to request additional resources when needed

Manage shared mailbox oversight and ensure equitable workload distribution across the team

Program Performance, Analytics & Continuous Improvement

Oversee creation and analysis of KPI reports within the REMS application to drive timely, data-informed prescriber outreach and prevent undue administrative burden

Monitor key REMS performance metrics and identify opportunities for operational improvement and stakeholder engagement enhancement

Analyze REMS stakeholder operations and interactions to identify process improvements that reduce administrative burden, increase efficiency, and enhance user experience

Conduct field observations of REMS Advisors during prescriber outreach and presentations; deliver constructive, actionable feedback to ensure clear and effective REMS education delivery

Synthesize data trends and translate insights into actionable recommendations to improve business procedures, practices, and stakeholder experiences

Provide feedback on technology enhancements to improve analytic tracking, reporting capabilities, and operational workflows; communicate recommendations to leadership

Design and facilitate workshops to share best practices, implementation insights, and lessons learned with REMS Advisors and healthcare professionals

Partner with cross-functional field teams (Sales, MSLs, Access) to promote REMS best practices and operational excellence initiatives that improve stakeholder efficiency

Lead monthly REMS review meetings with leadership to present program insights, customer feedback, trends, and improvement opportunities

Regulatory Compliance & Knowledge Management

Maintain comprehensive knowledge of Center of Excellence operations, including all Standard Operating Procedures (SOPs), work practices, and system functionalities

Develop, maintain, and implement REMS policies, procedures, and work practices in alignment with regulatory requirements and business needs

Stay current on FDA REMS regulations and industry trends; ensure internal teams and external stakeholders maintain compliance with regulatory requirements

Support internal audits and health authority inspections by providing documentation, insights, and subject matter expertise as required

Collaborate with Legal and Regulatory Strategy teams to ensure all communications and materials undergo appropriate RCR (Regulatory Content Review) process prior to distribution

Technology, Data Management & Cross-Functional Collaboration

Ensure accurate, current data is maintained in applicable systems used by REMS Advisors

Oversee and participate in User Acceptance Testing (UAT) for REMS technologies; report findings and recommendations to REMS IT personnel and leadership

Collaborate with department leadership to assess operational needs, establish project timelines, monitor implementation progress, and evaluate outcomes

Manage financial planning activities and ensure adherence to approved departmental budget

Deliver scheduled and ad-hoc reports to leadership as required to support strategic decision-making

Perform other duties as assigned to support departmental and organizational objectives

Skills/Knowledge Required :

Demonstrated ability to hire, coach, develop, and retain high-performing talent

Strong emotional intelligence with proven conflict resolution skills

Experience managing performance, including improvement plans and difficult conversations

Creates an environment of continuous learning and psychological safety for team members

Commitment to fostering an inclusive, collaborative team culture

Strong strategic orientation with ability to translate vision into operational priorities and actionable plans

Analytical and innovative thinker who identifies trends, insights, and process improvement opportunities

Problem solver who approaches situations holistically while prioritizing relationships and partnerships

Exceptional verbal and written communication skills with engaging public speaking ability

Ability to deliver complex REMS program information in a clear, concise, and compelling manner

Skilled at presenting data-driven insights and recommendations to leadership

Proficient with web-conferencing tools

Comprehensive understanding of FDA REMS regulations and industry best practices

Willingness to travel frequently as business needs require

Requirements:

Bachelor’s degree or equivalent with minimum of 5 years of pharmaceutical industry experience, required understanding of FDA REMS regulations a must. Demonstrated ability to manage, coach, and hire team members.

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:

Field - United States - US: $136,580 - $165,500


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.

U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits

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.

Candidate Rights

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

For roles based in Los Angeles County only:  If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:  https://careers.bms.com/california-residents/

For roles based in Washington State only: If you live in or expect to work from Washington State if hired for this position, please visit this page for important information about the Washington Fair Chance Act.

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at  https://careers.bms.com/fraud-protection .

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  TAEnablement@bms.com 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.

R1608427 : Senior Manager, REMS Advisor Lead

Job details

Seniority
Manager
Function
Medical Affairs
Therapeutic area
Not listed
Location
Field, United States
Employment type
Full time

How this role compares

Computed from every other active Medical Affairs role in our database, not just this employer's listings.

We currently track 399 comparable Manager Medical Affairs roles across 92 biopharma companies.

399Comparable roles tracked
374Currently active
92Companies hiring similar roles
47Countries represented

Salary context

98 of 399 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · PSL&D Compliance Training Ops & Business Lead (Manager) · Pfizer $88,500/yr – $147,500/yr
Peer group range $118,000 – $255,000 (median $186,375)

Where these roles are based

Top locations among the 399 comparable roles

United States142
China55
Japan36
India20
Germany18
United Kingdom12

+ 41 more countries

Seniority mix

399 of 399 peers have a known seniority level

Manager237
Associate Director86
Associate76

Therapeutic area mix

133 of 399 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology53
Neuroscience30
Immunology25
Rare Disease6
Cardiovascular / CVRM5
Vaccines & Infectious Disease4
Dermatology & Aesthetics4
Respiratory3
Gastroenterology2
Ophthalmology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
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60%similar
Regeneron Pharmaceuticals, Inc (USA) Sleepy Hollow, United States Manager
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Pfizer Cambridge, United States Manager
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Open in 3 locations

North Chicago, United StatesIrvine, United StatesFlorham Park, United States

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Medical Affairs job in the United States, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
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Function Therapeutic area Seniority Country
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Function Therapeutic area Seniority Country
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Neurocrine Biosciences Inc. · US CA San Diego, United States · Manager
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.