Associate Director EEE Governance

3 weeks ago


Hyderabad, India Novartis Full time

Job Description Summary #LI-Hybrid Primary Location: Hyderabad, India Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you Step into a pivotal role where your expertise will shape the future of scientific engagement at Novartis. As Associate Director EEE Governance, you’ll be at the forefront of implementing enterprise-wide standards and driving compliance across global medical affairs. You’ll collaborate with cross-functional teams to ensure ethical, impactful interactions with healthcare professionals and organizations, while influencing strategic decisions and enabling operational excellence. This is your opportunity to lead with integrity, innovate within a dynamic matrix environment, and make a meaningful difference in global health. Job Description Key Responsibilities - Support the Director, EEE Governance in designated therapeutic areas and deputize when needed - Implement Novartis standards and processes, ensuring alignment with evolving laws and strategies - Provide subject matter expertise on scientific engagement across global and regional teams - Review and guide scientific engagements in collaboration with Legal and ERC teams - Act as SME for Medical Affairs engagements like preceptorships and advisory boards - Serve as governance lead for international medical congresses, coordinating risk alignment - Deliver training on standards to internal teams and external partners, including new hires - Drive innovative scientific engagement solutions aligned with portfolio strategy - Oversee global congress sponsorships for regulatory and BeSure compatibility - Monitor HCP & HCO engagements to ensure quality, compliance, and risk mitigation Essential Requirements - University degree in Business Administration, Law, International Marketing, Communication, or Science - Minimum 8 years of experience in pharmaceutical HCP & HCO engagement and scientific education - Strong background in pharmaceutical compliance and governance environments - Excellent organizational, project management, and problem-solving skills - Proven ability to manage external vendors and build effective partnerships - Exceptional communication, interpersonal, and presentation capabilities - Experience in cross-functional collaboration and global team environments - High ethical standards with strong change management and stakeholder engagement skills Desirable Requirements - Experience working in a global pharmaceutical organization with complex matrix structures - Familiarity with international medical congress operations and compliance frameworks Skills Desired Clinical Data Management, Cross-Functional Team, Data Architecture, Data Governance, Data Management, Data Quality, Data Science, Data Strategy, Drug Development, Master Data, People Management, Waterfall Model



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