Global Medical Excellence Associate Director (GMEAD) (Remote)

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Requirements:

• Master’s degree plus 3 years’ experience in medical or clinical operational activities in the pharmaceutical industry.
• Strong prioritization and decision-making skills
• Proven ability to collaborate successfully with partners across functions and divisions in a matrix environment.
• Excellent interpersonal, analytical, and communication skills, both written and verbal, complemented by strong project management capabilities.
• Demonstrated business acumen with a comprehensive understanding of the pharmaceutical industry and healthcare landscape.
• Established track record of successful SL interaction.
• Deep knowledge of cross-functional working in a matrix environment in the pharmaceutical industry.

Responsibilities:

• Support lead GMED in the TA, which may include but is not limited to: Acting as primary liaison for SLs, actively engaging with a global network of contracted SLs within the relevant TA(s).Facilitating timely and positive interactions with these SLs to foster productive relationships.
• Support cross-functional SL engagement strategy that leads to clear lines of contact for SLs Coordinating cross-functional activities to ensure a smooth logistical experience for SLs contracted to perform several services on behalf of the company during major congresses, providing a One of our company's experiences while ensuring compliance with all relevant regulations.
• Managing strategic SL engagement for major global congresses to ensure cross-functional planning for on-site engagements and preparedness for non- of our company podium presentations.
• Leading the planning and execution of projects related to SL utilization, ensuring alignment with organizational priorities and goals.
• Providing the main point of contact for all country-to-country requests in the assigned TA(s), working with GDMA, RDMAs and home country medical to ensure appropriate speaker selection and efficient internal and external communication for medical activities where the request is for a commercial activity in the requesting country, include RCL and Human Health in initial discussion.
• Support cross-functional SL engagement strategy that leads to clear lines of contact for SLs Medical Approval Readiness Support lead GMED in the TA in partnering with EDMA/GDMA and cross-functional stakeholders to guide and coordinate medical activities in support of our global medical approval preparation planning with special focus on scientific leader engagement, scientific exchange priorities, key decision maker interactions, medical education, and policy/advocacy support (e.g. timelines, deliverables, human health (HH) communication, etc.
• Support lead GMED in the TA in strategic projects, which may include but is not limited to: Medical affairs-led cross-functional data gap strategy assessment to inform publication plans and other prioritized projects as deemed appropriate
• Serve as an active member of the TA Leadership Team for the assigned TA.
• Identify enterprise inefficiencies and develop strategies to address them.
• Exhibit expert understanding of company and organizational policies and procedures.
• Support lead GMED to partner with key cross-functional stakeholders and GMVC P&S to gather data for metrics and other requisite reports.