Cancer registrar Jobs in Boston, MA

Associate Director Medical Affairs Prostate Cancer

The Associate Director, Prostate Cancer develops scientific content and planning materials across Curium's radioligand, imaging, and oncology portfolio. This role partners with Medical Directors, Medical Affairs Operations, and cross-functional stakeholders to translate clinical and scientific information into clear, compliant deliverables that support medical planning, launch readiness, evidence generation, publications, congresses, training, and leadership decision-making. This is a hands-on role for a scientifically strong professional who combines scientific expertise, strong communication skills, and project management discipline to move work from strategy through execution. The ideal candidate will bring experience from a healthcare consulting, medical communications, or scientific communications environment and be comfortable supporting multiple stakeholders and projects simultaneously. The role offers an opportunity to gain increasing exposure to medical strategy development and cross-functional leadership, with potential growth into an Associate Medical Director position. This is a full-time U.S.-based role. Travel may be required for planning sessions, workshops, congresses, and team meetings.

Medical Planning 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.

Scientific Content 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.

Evidence Generation and Publications 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.

Execution and Coordination 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. Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e., FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.)

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. Close 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 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 an equal opportunity employer and believes everyone deserves respect, dignity and equality. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.