EPM Scientific is currently partnered with a leading pharmaceutical company to support the development of their Global Medical Affairs (GMA) strategy. This is a unique opportunity to contribute to global strategic initiatives and shape the medical direction of innovative compounds. Position: Global Medical Affairs Consultant Location: Euorpe, Remote Start Date: May/June (Flexible) Contract Type: Freelance/Consulting - 0.75 FTE, 12 Month Contract Language: English (additonal languages preferred) Therapeutic Area: Inflamation Key Responsibilities: Strategic Planning: Lead the development of global medical strategies across the asset lifecycle-from early development to post-launch-ensuring alignment with brand goals and scientific excellence. Cross-Functional Collaboration: Engage with internal stakeholders across Marketing, Clinical Development, Regulatory Affairs, Patient Engagement, RWE, Legal, and Digital to integrate medical insights into strategic planning. Medical Narrative & Evidence Generation: Develop the medical narrative to guide evidence generation and communication strategies. Support publication planning and data dissemination. Study Design & Oversight: Provide strategic input and oversight for Phase IV trials, Investigator-Initiated Studies (IIS), and Early Access Programs (EAPs). Medical Communications: Guide the creation of scientific content and ensure consistency across global medical communication platforms. Advisory Engagement: Plan and execute advisory boards, expert panels, and roundtables. Represent the company in scientific forums and patient engagement initiatives. Competitive Intelligence: Conduct medical landscape assessments, scenario planning, and competitive simulations to inform strategic decisions. Health Economics & Access: Contribute to the development of pharmacoeconomic value propositions and early access strategies for patients with unmet needs. Global-Local Alignment: Support regional and local medical teams in aligning their strategies with global objectives, including resource planning and launch readiness. Insight Generation: Collaborate with Key External Experts (KEEs) to gather insights that inform clinical development and brand strategy. Requirements: Proven experience in Global Medical Affairs within the pharmaceutical industry. Strong understanding of drug development, commercialization, and regulatory environments. Expertise in study design, data interpretation, and evidence generation. Excellent communication and stakeholder management skills. Ability to work independently and manage complex, cross-functional projects. Experience in competitive intelligence and strategic planning is highly desirable. If this opportunity aligns with your expertise and interests, please apply directly to learn more. If not, feel free to share with your network.