Associate Director, Scientific Communications - Cardiology

GE HealthCare

4d•$136,000 - $204,000•Onsite

About The Position

The Scientific Communication Associate Director, Radiopharmaceuticals US/CAN leads the operational backbone of the US Medical Affairs function within GMS, ensuring compliant, efficient, and high-quality execution of medical strategies across the PDx Radiopharmaceuticals care area portfolio. The role enables the delivery of medical accuracy of promotional and communication materials for the assigned care area (Oncology and Neurology), medical governance, training, publications and congress operations, and evidence execution support with a strong focus on operational excellence, cross-functional coordination, and audit readiness.

Requirements

Advanced scientific degree highly preferred (PharmD, PhD, MD, MSN, MPH, MSc, or similar).
5+ years of Medical Affairs or Medical Operations experience within the pharmaceutical, biotechnology, diagnostics, or imaging industry.
Demonstrated experience in medical review, medical information, medical governance, evidence operations, congress/publication operations, or medical systems/process management.
Demonstrated success leading AI and digital projects/programs in regulated environments.
Will not sponsor individuals for employment visas, now or in the future, for this job opening.
For U.S. based positions only, the pay range for this position is $136,000.00-$204,000.00 Annual.
Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
GE HealthCare will only employ those who are legally authorized to work in the United States for this opening.
Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).

Responsibilities

Develop, review, and approve scientific and educational materials for internal and external use (e.g., slide decks, training modules, educational brochures, Q&A documents), ensuring accuracy, balance, and compliance.
Lead or co-lead the Care Area(s) specific Medical Communication Plan at country level, ensuring that core scientific narratives, key messages, and FAQs are aligned with global/regional strategies and local needs.
Provide medical review and input for promotional materials in collaboration with care area leads and cross-functional review teams, ensuring scientific accuracy, fair and balanced information, and alignment with label, code, and company policies.
Oversee processes related to external material review, documentation governance, and cross-functional medical compliance.
Collaborate with colleagues from internal functions on cross-functional activities including Regulatory (e.g., on local label-related processes) and Market Access (e.g., on pricing, HTA, and other relevant dossiers).
Oversee operational processes supporting publications and congress planning in the US, aligned with global Strategy & Operations frameworks.
Ensure US operational compliance for publication planning, authorship documentation, evidence communication workflows, and post-congress reporting.
Maintain dashboards/reporting for publication progress, congress activities, and US medical communications workflows.
Partner with GMAPS S&O, Care Areas, Program and Functional leaders to embed AI into operating models, workflows, and decision-making processes.
Lead and co-lead care areas AI medical initiatives, including AI in Omnichannel communication, MSL / Field Medical Excellence, and automation of Medical Information & Publications.
Identify, collect, automate, and analyze data surrounding all facets of the scientific engagement model to inform ongoing areas of focus and priority.
Stay informed, curious, and report advancements of digital communication capabilities across the pharmaceutical and regulatory space.
Partner with business leaders to identify, prioritize, and activate high-value AI medical use cases, translating business problems into well-scoped opportunities for the teams.
Enable compliant and efficient external engagement by ensuring operational readiness of medical systems, tools, and processes (e.g., CRM/insights, congress management, publication tracking, SOP-guided processes).
Coordinate US presence at scientific congresses, ensuring alignment with global congress governance and impact-based planning.
Support US Medical Information (MI) operations, ensuring high-quality inquiry management, process compliance, accurate documentation, and timely response development, leading innovation in MI management with use of Global tools.
Oversee maintenance and governance of US medical content, including standard response letters, FAQs, and knowledge repositories.