Demo

Director, Medical Information and Review, Medical Affairs

Lantheus
Bedford, MA Full Time
POSTED ON 9/9/2025
AVAILABLE BEFORE 11/9/2025
Description

Lantheus is headquartered in Bedford, Massachusetts with offices in Canada, and Sweden. For more than 60 years, Lantheus has been instrumental in pioneering the field of medical imaging and has helped physicians enhance patient care with its broad product portfolio.

Lantheus is an entrepreneurial, agile, growing organization that provides innovative diagnostics, targeted therapeutics, and artificial intelligence (AI) solutions that empower clinicians to find, fight and follow disease. At Lantheus our purpose and values guide our behaviors in all interactions and play a vital role in creating a dynamic environment that contributes to our success. Every employee is crucial to our success; we respect one another and act as one knowing that someone's health is in our hands. We believe in helping people be their best and are seeking to bring together a diverse group of individuals with different viewpoints and skill sets to be a part of a productive and inclusive team.

This position is onsite and requires a presence on-site of three days per week in Bedford, MA.

Summary of Role

The Director of Medical Information and Medical Review is a strategic team leader who will oversee all aspects of Medical Information and Medical Review across Lantheus' oncology, cardiology, and neurology portfolio. The Director will manage a high-performing team, oversee the Medical Information Call Center, and collaborate cross-functionally to strategically support product lifecycle communications and uphold the integrity of scientific messaging. This role also leads the team responsible for Medical Review of promotional, non-promotional, and medical materials, ensuring scientific accuracy, regulatory compliance, and strategic alignment.

Strategic Direction

  • Define and execute the strategic vision for the Medical Information & Review function
  • Lead and develop a high-performing team of medical information specialists and reviewers
  • Stay ahead of industry trends and integrate best practices to continuously evolve the function

Medical Information Leadership

  • Oversee Call Center and resource deployment across medical information
  • Ensure timely and effective responses to inquiries from healthcare professionals, patients, and internal stakeholders
  • Lead the development and maintenance of the MI database, Standard Response Documents (SRDs) and FAQs across oncology, cardiology, and neurology
  • Analyze trends in medical inquiries to inform strategic insights and content updates

Medical Review Oversight

  • Oversee medical review of promotional, non-promotional, and medical materials as part of the Medical, Legal, and Regulatory review process
  • Ensure all reviewed materials are scientifically accurate, balanced, and consistent with approved product labeling, where applicable
  • Collaborate with Regulatory and Legal to ensure compliance with internal, FDA, and other global regulatory standards

Cross-Functional Collaboration

  • Serve as a strategic advisor with cross-functional colleagues including Pharmacovigilance, Clinical Development, Medical Affairs, Regulatory, Legal, Compliance, and Commercial to ensure alignment and audit readiness
  • Support global harmonization and adoption of medical information practices and review standards

Technology and Process Optimization

  • Manage external vendors for call center operations and medical content development
  • Drive implementation of technology solutions (e.g., Veeva Vault) to enhance review efficiency and content management
  • Continuously evaluate and improve MI and MLR processes for scalability and compliance

Basic Qualifications

  • Doctorate Degree (PhD, PharmD, MD, or equivalent)
  • 5 or more years of relevant experience in Medical Affairs including at least 2 years in Medical Information within the pharmaceutical/ biopharmaceutical industry
  • Two or more years of previous leadership within a function and experience managing direct reports
  • Strong knowledge of global regulatory and compliance guidelines governing medical information and review activities
  • Excellent communication and interpersonal skills with the ability to work collaboratively across various departments
  • Strong analytical budget and vendor management skills

Other Requirements

  • Preferred experience in radiopharmaceuticals
  • Preferred experience in oncology or neurology

Core Values

The ideal candidate will embody Lantheus core values:

  • Let people be their best
  • Respect one another and act as one
  • Learn, adapt, and win
  • Know someone's health is in our hands
  • Own the solution and make it happen

Lantheus is an equal opportunity employer that provides a workplace free from discrimination. All qualified applicants and employees are considered without regard to race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any other characteristic protected by law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Lantheus Talent Acquisition team at talentacquisition@lantheus.com.



Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.



Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities


 

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