We use cookies. Find out more about it here. By continuing to browse this site you are agreeing to our use of cookies.
#alert
Back to search results
New

Director Medical Information

Curium Pharma
flexible benefit account, paid time off, 401(k), retirement plan
United States, New Jersey, New Brunswick
Mar 26, 2026

Director Medical Information
Date:

Mar 25, 2026
Location:


New Brunswick, NJ, United States, 63146



About Curium

Curium is the world's largest nuclear medicine company with more than a century of industry experience. We develop, manufacture and distribute world-class radiopharmaceutical products to help patients around the globe. Our proven heritage combined with a pioneering approach are the hallmarks to deliver innovation, excellence and unparalleled service.

With manufacturing facilities across Europe and the United States, Curium delivers SPECT, PET and therapeutic radiopharmaceutical solutions for life-threatening diseases to over 14 million patients annually. The name 'Curium' honors the legacy of pioneering radioactive researchers Marie and Pierre Curie, after whom the radioactive element curium was named and emphasizes our focus on nuclear medicine. The tagline 'Life Forward' represents our commitment to securing a brighter future for all those we serve: An enhanced quality of care for our patients. A trusted partner to our customers. A supportive employer to our valued team.


Summary of Position

The Lead of Medical Information will establish and lead the Medical Information function at Curium NA, building infrastructure and processes to support the upcoming launch of our novel RLT. This leader will design and implement MI strategy, develop standard operating procedures, and recruit and manage a small team to deliver high-quality medical information services. The role requires strong cross-functional collaboration, scientific expertise, and operational excellence to ensure compliant and customer-focused information exchange.



This a remote position and the candidate can live anywhere in the US. Regular travel required (up to 25%).

Essential Functions

  • Strategy & Leadership

    • Define and implement the Medical Information strategy aligned with company objectives and product launch timelines.
    • Build, lead, and mentor a small Medical Information team to deliver high-quality, customer-centric service.
    • Develop KPIs and performance measures for the function.


  • Medical Information Operations

    • Establish systems, databases, and workflows for medical inquiry management.
    • Develop and maintain standard response documents (SRDs), FAQs, and medical content to support field and contact center responses.
    • Ensure consistent, accurate, and compliant communication of medical information to healthcare professionals, patients, and other stakeholders.
    • Implement processes for capturing, analyzing, and reporting inquiry trends to inform medical strategy and evidence generation.


  • Compliance & Quality

    • Ensure all Medical Information activities comply with company SOPs, regulatory requirements, and industry standards.
    • Partner with Legal, Compliance, and Regulatory Affairs to ensure rigorous review and approval of medical information materials.
    • Train internal stakeholders on appropriate use and escalation of medical information resources.


  • Cross-Functional Collaboration

    • Collaborate with Medical Affairs, Pharmacovigilance, Market Access, and Commercial teams to ensure seamless information flow and aligned communication.
    • Partner with Clinical Development and HEOR to integrate evolving evidence into medical information resources.
    • Provide insights from inquiries to Medical Affairs leadership to guide strategy, publications, and education initiatives.



Requirements

  • Advanced degree (PharmD, PhD, MD, or equivalent) required.
  • 5+ years of relevant pharmaceutical industry experience, including substantial experience in Medical Information.
  • Strong knowledge and experience in nuclear medicine and/or oncology, esp. prostate cancer preferred
  • Proven track record of building or scaling a Medical Information function, ideally in oncology or nuclear medicine.
  • Strong knowledge of regulatory and compliance requirements (FDA, OIG, PhRMA, ICH).
  • Experience in preparing for and supporting product launches, preferably in oncology or radiopharmaceuticals.
  • Excellent leadership, people management, and organizational skills.
  • Ability to thrive in a fast-paced, small-company environment with hands-on execution.



Curium offers a generous benefits package for eligible employees as follows:


Medical


Dental


Vision


Health Care Flexible Spending Account


Dependent Care Flexible Spending Account


Health Savings Account


Basic Life and AD&D Coverage


Voluntary Life and AD&D Coverage


Short-Term Disability


Long-Term Disability


Voluntary Long-Term Disability Buy-Up


Norton LifeLock


Nationwide Pet Insurance


Employee Assistance Program


Paid Time Off


Fixed & Floating Holidays


401k Retirement Plan

Competencies

Disclaimer

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.

Equal Opportunity Employer

Curium is anequal opportunity employerand believes everyone deserves respect, dignity and equality.All applicants will be considered for employmentwithout attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.






Job Segment:
Compliance, Medical Technologist, Oncology, Pharmaceutical, Regulatory Affairs, Legal, Healthcare, Science

Applied = 0

(web-bd9584865-ksnsn)