Associate Director Medical Affairs Prostate Cancer

Essential Functions

• Partner with Medical Directors and Medical Affairs leadership to develop medical plans, launch and tactical plans, project timelines, and leadership presentations.
• Translate medical strategy and leadership direction into clear actions and deliverables.
• Develop and update scientific platforms, slide decks, executive briefings, workshop materials, training materials, congress materials, and medical education content.
• Translate clinical data and scientific evidence into accurate, audience-appropriate content.
• Work with subject matter experts to maintain consistent scientific narratives, messages, and supporting evidence.
• Conduct literature, evidence, and competitive landscape reviews.
• Support publication planning, evidence gap assessments, advisory boards, and consultant meetings.
• Create evidence summaries, briefing documents, reference packs, and executive reports.
• Manage multiple projects, stakeholders, review cycles, and deadlines simultaneously.
• Partner with Medical Affairs, Clinical Development, Medical Information, HEOR, Publications, Regulatory, Compliance, Commercial, and external agencies as appropriate.
• Develop dashboards in Power BI, Tableau, or similar tools to track Medical Affairs activities, timelines, and metrics.
• Maintain strong version control, source documentation, and organized files.
• Identify practical ways to improve the quality, consistency, and speed of Medical Affairs deliverables.

Requirements

• Advanced degree in a scientific or clinical discipline required, such as a PharmD, PhD, MD, or relevant MS.
• 12 or more years of experience in healthcare consulting, medical communications, scientific communications, or Medical Affairs.
• Agency or consulting experience strongly preferred.
• Experience managing multiple scientific projects, stakeholders, review cycles, and deadlines in a consulting, agency, or Medical Affairs environment.
• Experience developing scientific and strategic deliverables, including medical plans, scientific platforms, slide decks, executive presentations, publication materials, workshop content, and other client-facing materials.
• Experience in oncology, radiopharmaceuticals, or nuclear medicine preferred.

Core Competencies

• Strong scientific writing and communication skills.
• Ability to understand and simplify complex clinical and scientific information.
• Ability to independently develop scientific content and drive projects from concept through execution.
• Strong organization, attention to detail, and follow-through.
• Ability to work independently and manage competing priorities.
• Advanced PowerPoint skills.
• Experience using Power BI, Tableau, or similar tools to develop dashboards and communicate insights.

Working Conditions

• Standard office environment.
• Willingness to work in a team-based environment.
• Closed attention to detail required.
• Must be able to work outside of regular work hours.
• Up to 25% travel required.
• Remote work acceptable with frequent trips to the St. Louis office.