Associate Director Global Medical Affairs CRM, Renal

Experteer Overview

You will manage complex assets with pharmacovigilance needs and represent GMA to senior stakeholders in a global, agile environment. You help ensure high medical quality and impactful medical insights across disease areas.

• Lead development and execution of medical affairs strategy for TA/asset priority programs
• Co-develop plans for evidence generation, MSL/Field Medical Affairs strategy, medical education, publication planning, and expert networks
• Co-own development and implementation of innovative education and scientific communication plans for external stakeholders
• Track finances to ensure timely, cost-effective medical activity execution
• Prepare SRC submissions for TA assets within remit
• Collaborate with Development, S&G, US and International teams to shape portfolio and diversify evidence
• Represent GMA with internal and external audiences alongside TAs and regulatory partners
• Advocate for the patient perspective in decision making
• Provide direction on reimbursement and market-access strategies
• Contribute proactive input on new therapeutic indications to enrich registration programs
• Ensure Patient Access programs are supported across brands and compliant
• Deliver proactive medical input to asset lifecycle management for new opportunities
• Maintain compliance of GMA activities with policy guidelines and medical quality standards
• Support cross-functional, cross-market collaboration in an agile organization

• MD (Nephrologist preferred) or PhD/PharmD in Health Sciences
• 5+ years in Medical Affairs and/or Clinical Development, preferably in renal diseases
• Strong ability to navigate uncertainty with minimal supervision
• Fluent in English (written and spoken); other languages advantageous
• Strategic mindset with credibility to influence in a matrix organization
• Proven collaboration across functions and markets to achieve shared outcomes
• Deep understanding of health care systems and nephrology stakeholders
• Track record delivering medical affairs projects on time and with quality (advisory boards, publications, study development)
• Experience developing and implementing innovative programs and processes
• Understanding of unmet medical needs and ability to generate relevant evidence using multichannel communication
• Reputable external credibility as a peer expert
• Agile mindset with capability to lead in a multi-disease, global setting
• Knowledge of GCP, scientific/clinical methods, protocols, and regulatory requirements for clinical studies

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