Pallavi Dhillon

Pallavi Dhillon is a performance-driven Clinical Research and Pharmacovigilance professional with over 12 years of experience spanning clinical operations, project management, pharmacovigilance, and regulatory compliance across global and Indian markets. Currently serving as Clinical Operation Manager (Project Manager) at Veeda Clinical Research Ltd., she specializes in overseeing end-to-end clinical trial management, from site activation to study closeout, while ensuring GCP/ICH compliance and stakeholder satisfaction.

Expertise covers project leadership, study start-up, patient recruitment, central and on-site monitoring, data management, vendor oversight, and quality/audit readiness. I worked extensively across diverse therapeutic areas, including oncology, cardiovascular, immunology, CNS, diabetes, Rare Disease and metabolic disorders, 

With advanced qualifications including a Ph.D. in Pharmaceutics (Jamia Hamdard, New Delhi), an M.Pharm. (Pharmaceutics), and an M.Sc. in Clinical Research (Cranfield University, UK), a strong academic foundation coupled with practical leadership in clinical research.

Having strategic vision, stakeholder engagement, and risk-based project management, she has successfully led cross-functional teams, managed sponsor/CRO/vendor collaborations, and driven process improvements to enhance trial efficiency and data quality.

I am currently working as Clinical Operation Manager (Project Manager) at Veeda Clinical Research Ltd. (2024–present), where leads cross-functional teams, oversees project planning, and ensures GCP/ICH compliance across clinical trials. Prior to this, served as a Project Manager at CliniExperts Research Pvt. Ltd. (2023–2024), managing end-to-end study operations, vendor oversight, and patient recruitment strategies. From 2018 to 2023, worked with Trans Atlantic Therapeutics as Team Lead – Clinical Research Operations, driving Phase 3 and IIT trials with a strong focus on oncology. Earlier, held the position of Senior Clinical Associate at Clinfomatrix (2016–2018), ensuring smooth site management and regulatory compliance, and worked with GlobalPharmatek LLC (2012–2016) as a Clinical Research Associate, supporting trial documentation and monitoring. My foundation in pharmacovigilance was built through roles at Baxter Healthcare (2009–2012) and Pfizer (2009), where responsible for safety case processing, regulatory submissions, and compliance.Started her journey in clinical research with Sir Ganga Ram Hospital (2008–2009) and Clinsys Clinical Research (2008) Indian Council of Medical Research (2006–2007) as a Research Associate.  

PhD Pharmaceutics, M.Pharm, M.Sc Clinical Research UK, B.Pharm