Puneeth Mandaknallikar
About Puneeth Mandaknallikar
Puneeth Mandaknallikar is a Senior Manager at Bristol Myers Squibb in India, with extensive experience in clinical research and regulatory compliance.
Title and Current Role
Puneeth Mandaknallikar is currently employed as a Senior Manager at Bristol Myers Squibb in India, utilizing a hybrid work format. In this role, he leverages his extensive experience in clinical research and project management to oversee various initiatives and ensure that deliverables are met efficiently within stipulated timelines.
Previous Experience at GSK
Prior to his current position, Puneeth Mandaknallikar worked at GSK in multiple capacities. From 2022 to 2023, he served as a Senior Study Delivery Lead, and from 2021 to 2022, he held the position of Study Delivery Lead (Global Project) in Bengaluru, Karnataka, India. During his tenure, he was responsible for managing global projects and ensuring the successful delivery of clinical studies.
Career at Sami-Sabinsa Group Limited and Covance
Before joining GSK, Puneeth Mandaknallikar was a Project Manager at Sami-Sabinsa Group Limited from 2019 to 2021 in Bangalore. He also served as an Assistant Manager at Covance from 2018 to 2019 in Bengaluru, Karnataka, India. In these roles, he played a crucial part in project management, clinical trial operations, and quality assurance, contributing to drug development and safety life cycle management.
Educational Background
Puneeth Mandaknallikar holds an M.Sc in Clinical Research from Cranfield University in the UK, completed between 2006 and 2008. He also achieved a PGDBM in Business Management from ICRI Bangalore in 2007. Earlier in his academic journey, he earned an MSc in Biotechnology from City College, Bangalore, and a BSc in Biotechnology from East West First Grade College of Science, Bangalore.
Publications and Mentorship
Puneeth Mandaknallikar is a published author with works focusing on clinical research and regulatory compliance. He is also actively involved in mentoring upcoming professionals in clinical research through various programs. His expertise includes remote monitoring, signal detection within clinical trials, and workload management. He has played a significant role in regulatory-safety competency development throughout his career.