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Medical Director - Prostate Cancer

Curium Pharma
United States, Missouri, St. Louis
111 West Port Plaza Drive (Show on map)
Oct 09, 2025

Medical Director - Prostate Cancer
Date:

Oct 9, 2025
Location:


St. Louis, MO, United States



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 Medical Director - Prostate Cancer will be a key member of the medical brand team and serve as one of the primary medical leaders supporting the prostate cancer therapy launch in the U.S. This role will provide medical expertise to guide the development and execution of the medical strategy, including the medical launch plan, ensure alignment with clinical development and commercial initiatives, and drive evidence-based education and communication to internal and external stakeholders.



Work Schedule: Monday - Friday 8am-5pm

Essential Functions

  • Collaborate with the Medical Team Leader to develop and implement the medical strategy for the prostate cancer brand.
  • Serve as a medical expert on prostate cancer, including current standards of care, emerging therapies, and clinical trial data.
  • Provide medical guidance for brand planning, ensuring alignment with scientific, clinical, and regulatory standards.
  • Support medical communication and education initiatives for internal teams, healthcare providers, and key opinion leaders (KOLs).
  • Engage with KOLs, advisory boards, and scientific experts to inform brand strategy and generate actionable insights.
  • Review and approve medical content for promotional and non-promotional materials, ensuring scientific accuracy and compliance.
  • Collaborate cross-functionally with commercial, clinical development, regulatory, and health economics teams to support product lifecycle planning.
  • Support commercial launch activities as a medical subject matter expert.
  • Monitor scientific and clinical developments in prostate cancer and translate insights into actionable medical strategy.

Requirements

  • MD, DO, PhD, PharmD, or equivalent medical degree required; specialty in oncology, urology, or nuclear medicine preferred.
  • 12 or more years of relevant experience and knowledge in medical affairs, preferably in oncology, urology, or nuclear medicine.
  • Strong understanding of clinical development, regulatory requirements, the healthcare and business environment, and the pharmaceutical/biotech industry.
  • Demonstrated experience engaging with KOLs, advisory boards, and medical societies.
  • Excellent communication, presentation, and interpersonal skills.
  • Ability to work collaboratively in a cross-functional team environment and influence stakeholders.
  • Experience launching or managing oncology brands in the U.S. preferred.
  • Substantial experience and knowledge in prostate cancer preferred.



Working Conditions:



  • This position will work in typical office conditions with extensive time using personal computer equipment.
  • May be required to sit or stand for long periods of time while performing duties.
  • Close attention to detail required.
  • Willingness to work in a team-based environment.
  • The position deals with many deadlines. Due to the short turnaround time of deadlines and limited time, overtime, weekend work and holiday work is sometimes required.
  • Ability to travel domestically and potentially Internationally as required.

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.






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