Director, Platform Enablement RLT & RLI (US Medical) 2 of 2

Role Summary

Director Platform Enablement, Radioligand Therapy (RLT) and Radioligand Imaging (RLI) within US Medical Affairs. Focused on executing large-scale strategic initiatives to enable RLT and RLI enablement across treatment archetypes, aligning multiple workstreams to remove barriers to appropriate patient treatment. Reports to the Head of RLT Enablement and collaborates with US and global cross-functional teams.

Responsibilities

• Demonstrate expertise in implementing education strategies to support platform and disease education at large scale; build partnerships with Medical, General Management/Commercial, and US/Global colleagues.
• Collaborate with Medical Strategy Teams (MST) and Integrated Product Strategy Team (IPST) to drive product strategy.
• Provide input and lead execution of platform-level initiatives during launch planning and post-launch.
• Educate colleagues and health care professionals to support platform strategy.
• Explore, plan, and implement innovative communications solutions, including digital channels, to address strategic and scientific gaps.
• Support development of a strong medical engagement plan with diverse Medical functions and capabilities.
• Foster relationships with National, Regional, and Local Medical Experts, including Investigators; support Medical Expert Engagement Strategy.
• Plan, execute, and support advisory boards; work with Field Medical on insight-gathering initiatives.
• Develop positive relationships with Global colleagues and cross-functional teams.

Qualifications

• Minimum 5 years in pharmaceutical, biotech, or Radioligand therapy/imaging.
• Experience leading large-scale business planning processes with clear goals and metrics.
• Minimum 5+ years in product strategy/medical communication or relevant Medical Affairs roles in US biotech/pharma, medical education agencies, or academic/clinical settings.
• Oncology therapeutic area knowledge preferred; experience interacting with HCPs/researchers at US academic centers.
• Direct clinical research experience in operations; understanding of clinical trial operations and patient recruitment solutions and educational tools.
• Proven ability to build trusting relationships with Medical Experts and Investigators.
• Established relationships with US Medical Experts and US Professional Societies; experience planning and leading external meetings.
• Strong track record of managing cross-functional projects; ability to collaborate with diverse teams.
• Excellent interpersonal, relationship management, and presentation skills.
• Demonstrated problem-solving skills; comfortable with complexity; US experience preferred.

Education

• Advanced degree in scientific/medical/health discipline required.
• Master‚Äôs degree preferred.