Abna Sreedhar Vysiapat
EMEA Medical Affairs Coordinator @ Aerogen
About
I am a Pharma professional with a MSc in Pharmaceutical Business & Technology from Griffith College, Dublin, and a Master of Pharmacy in Quality Assurance from BNCP, Mumbai. With 7+ years of experience across pharmaceutical and healthcare domains, I have contributed to global organizations including Pfizer and Sanofi, working in cross regional, multicultural environments. During my time at Pfizer India as EM & China Medical Excellence Coordinator, I led the end-to-end implementation of a global SharePoint platform—creating a unified knowledge and content hub for Pfizer Emerging Markets colleagues across 100+ countries and four continents. This initiative improved collaboration, standardized processes, and enhanced information accessibility across medical teams worldwide. At Sanofi, I played an active role in successfully meeting compliance standards during the 2019 Sanofi Global Audit, demonstrating my dedication to quality, operational discipline, and continuous improvement. My expertise spans GMP operations, Lean Six Sigma principles, audit readiness, KPI tracking, and digital tools such as Tableau, SharePoint, and the Microsoft Office suite. I thrive in environments that require structured planning, cross-functional collaboration, data driven decision-making, and operational excellence. Professionally, I am inspired by roles at the intersection of Project Management, Operational Excellence, Medical Operations, and Quality & Compliance. I am known for my collaborative mindset, attention to detail, and drive to deliver high quality outcomes. Outside work, I enjoy creating mandala art, reading thrillers, and volunteering for social causes—activities that help me stay creative, grounded, and connected to community impact.
Ireland
Dublin
Pharmaceuticals
Digital Twins, Quality Assurance, Analytical Method Validation, Analytical Methods Development, Pharmaceutical Formulation, Clinical Trials, AI in Clinical Trials, Artificial Intelligence (AI), AI in Pharma, Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), Quality System, Medical Assisting, Caregiving, Manual Handling, Care of Older People, Project Management, Data Analysis, KOL engagement, Strategic Planning
Experience

Healthcare Assistant
Dublin, County Dublin, Ireland
In my role as a part-time healthcare assistant, I comply with Standard Operational Policies and Procedures as documented in the Homes Quality Manual. Perform proper manual handling and patients moving at every task., complied with the Health and Safety procedures at work at all the times to prevent injuries. Help in promoting the mobility of residents, supervising and assisting as necessary to ensure optimum mobility is maintained and improved where possible. I also assist them with personal care and medicine reminders.

Project Coordinator-interim (Site Coordinator)
Mumbai Metropolitan Region, India
Coordinated daily on-site activities, ensuring adherence to project plans and schedules. Monitored and managed site resources, including labor, materials, and equipment. Prepared and submitted regular reports on project status, including progress updates, resource utilization, and risk assessments.

EM & China Medical Excellence Coordinator
Mumbai, Maharashtra, India
In my role as EM & China Medical Excellence Coordinator at Pfizer India, I orchestrate the monthly analysis and reporting of critical metrics, ensuring accurate and insightful information for medical excellence leadership. Collaborating closely with Medical Excellence Leadership, I present process workflows, providing valuable insights into our operational efficiency. My notable achievements include: -Implementing process enhancements across Content Development, Review, Evidence Generation, and Launch Excellence teams, showcasing my strategic impact on key divisions. -Implemented a SharePoint site, establishing a unified information hub for Pfizer Medical colleagues across 100+ countries and 4 continents -Formulating a detailed project plan for Emerging Market SharePoint, achieved through collaborative efforts with the digital team. -Successfully facilitating over 300 GDMS system uploads for various non-interventional studies

Project Coordinator - Medical affairs
Mumbai, Maharashtra, India
In my role as Project Coordinator, I supported the Senior Manager, facilitating the engagement of over 50 Healthcare Professionals (HCPs) for Continuing Medical Education (CME) and Publication projects. My dedication to ensuring seamless coordination across divisions significantly contributed to the smooth execution of Key Opinion Leader (KOL) activities. Additionally, I effectively coordinated and managed scientific activities with Pharma Multinational Corporation (MNC) clients and vendors, fostering successful collaborations. My commitment to data accuracy and currency is evident in my role, where I meticulously maintained updated records on various HCPs and projects. As part of my key initiatives, I developed and presented numerous proposals for scientific activities, establishing valuable connections with HCPs and Scientific societies across diverse therapy areas. This proactive approach showcases my strategic vision and dedication to advancing impactful scientific initiatives.

Executive Medical Governance and Medical Excellence
Mumbai Area, India
In this role, I supported the medical team in overseeing approvals for crucial HCP, HCO, and MSA interactions. I was responsible for conducting thorough analysis adhering to compliance and audit recommendations. I effectively documented reviews for local event HCP and HCO/MSA engagements and also collaborated with the ITS team for system changes and simplification. I actively participated and provided support during the Sanofi Global Audit in December 2019. Furthermore, I successfully completed training on Veeva PromoMats.
Education

Pharmaceutical Business & Technology
- Modules- Clinical Research Management (Drug development lifecycle, clinical research & trials, Clinical trial operations, future trends in clinical research) - Processes, Production and Pharmaceutical Quality Systems (Validation life cycle) - Regulatory landscape of Pharmaceutical Business (Clinical trials regulation, waste management) - Pharmaceutical Technology Transfer (Analytical method transfer, process validation) - 21st Century Dynamics & Emerging trends (Innovative medicines, patient outcomes, BGIE, future definition of quality management) - Research methods (Process, quantitative & qualitative methods, product management) - Operational Excellence & the Science of Innovation (Lean enterprise, Six Sigma & KPI) - Strategy, Leadership & the Culture of Innovation (Strategic thinking in achieving technological innovation, corporate governance & business ethics)
Abna Sreedhar Vysiapat's Contact Information
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