Senior Director, Managed Access Programs, Medical Evidence Generation
Senior Director, Managed Access Programs, Medical Evidence Generation

Senior Director, Managed Access Programs, Medical Evidence Generation

Uxbridge Full-Time 72000 - 108000 £ / year (est.) No home office possible
L

At a Glance

  • Tasks: Lead global Managed Access Programs to ensure patient access to innovative medicines.
  • Company: Join Bristol Myers Squibb, where meaningful work transforms lives every day.
  • Benefits: Enjoy a hybrid work model, competitive benefits, and resources for personal and professional growth.
  • Why this job: Make a real impact on health equity while collaborating with diverse, high-achieving teams.
  • Qualifications: 7+ years in pharma/biotech with expertise in managed access and regulatory compliance required.
  • Other info: BMS values diversity and offers accommodations for applicants with disabilities.

The predicted salary is between 72000 - 108000 £ per year.

Job Title: Senior Director, Managed Access Programs, Medical Evidence Generation

Job Location: Uxbridge, UK

Job Location Type: Hybrid

Job Contract Type: Full-time

Job Seniority Level: Director

Working with Us

Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Position Summary

The Senior Director, Managed Access Programs (MAPs) will be responsible for partnering to develop the strategy and lead the global implementation and management of Managed Access Programs across multiple disease areas. This role supports the company’s health equity ambition, ensuring that patients with unmet needs receive access to our innovative medicines in a compliant and ethical manner. The MAPs Lead will provide strategic input, oversight, and coordination to ensure a streamlined and efficient approach to managed access and ensure equity, sustainability, scalability, and appropriate data capture across their respective disease areas. She/He will work closely with cross-functional teams ensuring the implementation of appropriate policies, processes, and systems that support the centralized managed access strategy. Additionally, this role will be accountable for ensuring compliance with country-specific regulations and effective data capture.

This role reports to the Executive Director, Managed Access.

Key Responsibilities

Strategic Planning

  • Collaborate with key partners (WW TA, DD, legal, compliance, RCO, Country medical teams) to define and develop the managed access strategy for assets across multiple diseases TAs.
  • Ensure the managed access strategy has input from all required partners and goes through the appropriate review and governance processes.

MAP Oversight

  • Partner with GDO/RCO to ensure seamless operationalization of managed access programs for their respective disease areas, ensuring appropriate country rules are followed.
  • Implement standardized policies, procedures, and best practices across the portfolio of managed access programs.
  • Establish & track key performance indicators (KPIs) to measure the success of the managed access programs and leverage data and analytics to optimize MAPs and accelerate impact.

Cross-Functional Collaboration
Serve as the primary point of contact for internal (Medical Affairs, Development, Commercial, Regulatory Affairs, Legal, and Compliance) and external stakeholders to ensure seamless program execution and compliance with global, regional, and local regulations and guidelines.

Data Capture and Evidence Generation

  • Optimize the capture and utilization of data and evidence from MAPs that appropriately supports the value of BMS’ assets and ensure that data collection processes comply with country-specific regulations and privacy laws.

Training and Support
Provide training and support to internal teams on MAP processes and best practices.

Innovation
Foster an innovative culture and lead initiatives to increase innovative approaches to MAPs.

Qualifications & Experience

  • Educational Background: Degree in a relevant field (e.g., Life Sciences, Patient Access, Pharmacy, Public Health) required.
  • Industry Experience: Minimum of 7+ years of experience in the pharmaceutical or biotechnology industry, with at least 3 years in a role related to managed access. Proven track record of successfully managing MAPs across a disease area.
  • Regulatory / Compliance Knowledge: In-depth knowledge of global and local regulations and guidelines related to Managed Access Programs.
  • Communication Skills: Excellent communication and interpersonal skills, with the ability to influence and collaborate effectively across functions and levels.
  • Strategic Thinking: Strategic thinker with strong analytical and problem-solving abilities.
  • Adaptability: Ability to work in a fast-paced, dynamic environment and manage multiple priorities.

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers

With a single vision as inspiring as Transforming patients’ lives through science, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role. Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

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 . Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

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

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.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

#J-18808-Ljbffr

Senior Director, Managed Access Programs, Medical Evidence Generation employer: Lifelancer

At Bristol Myers Squibb, we offer a unique opportunity to work in a dynamic and inclusive environment where your contributions can truly make a difference in patients' lives. Our hybrid work model promotes flexibility, while our commitment to employee growth ensures that you will have access to diverse career development opportunities. Join us in Uxbridge, UK, where you can collaborate with high-achieving teams and be part of a culture that values innovation, accountability, and the pursuit of health equity.
L

Contact Detail:

Lifelancer Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Director, Managed Access Programs, Medical Evidence Generation

✨Tip Number 1

Familiarize yourself with the latest trends and regulations in Managed Access Programs. Understanding the nuances of compliance and data capture will not only help you in interviews but also demonstrate your commitment to the role.

✨Tip Number 2

Network with professionals in the pharmaceutical and biotechnology industries, especially those involved in managed access. Engaging with these individuals can provide insights into the role and may even lead to referrals.

✨Tip Number 3

Prepare to discuss specific examples of how you've successfully managed MAPs in the past. Highlighting your strategic thinking and problem-solving abilities will set you apart from other candidates.

✨Tip Number 4

Showcase your ability to collaborate across functions by preparing examples of past cross-functional projects. This will illustrate your interpersonal skills and your capacity to work effectively within diverse teams.

We think you need these skills to ace Senior Director, Managed Access Programs, Medical Evidence Generation

Strategic Planning
Cross-Functional Collaboration
Regulatory Compliance Knowledge
Data Capture and Evidence Generation
Performance Measurement and KPI Tracking
Training and Support
Analytical Skills
Problem-Solving Skills
Excellent Communication Skills
Interpersonal Skills
Adaptability
Experience in Managed Access Programs
Knowledge of Global and Local Regulations
Ability to Influence and Collaborate Effectively

Some tips for your application 🫡

Understand the Role: Take the time to thoroughly read the job description for the Senior Director, Managed Access Programs. Understand the key responsibilities and qualifications required, and think about how your experience aligns with these.

Tailor Your CV: Customize your CV to highlight relevant experience in managed access programs, strategic planning, and cross-functional collaboration. Use specific examples that demonstrate your success in similar roles.

Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also reflects your passion for transforming patients' lives through science. Mention how your values align with those of Bristol Myers Squibb.

Highlight Compliance Knowledge: Emphasize your understanding of global and local regulations related to Managed Access Programs. This is crucial for the role, so provide examples of how you've navigated compliance in previous positions.

How to prepare for a job interview at Lifelancer

✨Understand the Managed Access Programs Landscape

Familiarize yourself with the current trends and challenges in Managed Access Programs. Be prepared to discuss how you can contribute to Bristol Myers Squibb's health equity ambition and ensure compliance with regulations.

✨Showcase Your Strategic Thinking Skills

Prepare examples that demonstrate your ability to develop and implement strategic plans. Highlight your experience in collaborating with cross-functional teams and how you've successfully managed MAPs in the past.

✨Emphasize Communication and Collaboration

Since this role requires working with various stakeholders, be ready to discuss your communication style and how you build relationships across different functions. Share specific instances where your interpersonal skills made a difference.

✨Demonstrate Adaptability and Problem-Solving

The pharmaceutical industry is fast-paced and dynamic. Prepare to discuss how you've navigated challenges in previous roles and your approach to managing multiple priorities effectively.

Senior Director, Managed Access Programs, Medical Evidence Generation
Lifelancer
L
  • Senior Director, Managed Access Programs, Medical Evidence Generation

    Uxbridge
    Full-Time
    72000 - 108000 £ / year (est.)

    Application deadline: 2027-03-14

  • L

    Lifelancer

Similar positions in other companies
Europas größte Jobbörse für Gen-Z
discover-jobs-cta
Discover now
>