Pramod Kashid
Senior Director, Clinical Trial Management
Currently, Dr. Pramod Kashid is working as a Senior Director for clinical trial management at Medpace, one of the leading clinical research organizations founded in 1992 and
publicly listed on the NASDAQ in 2016 as Medpace Holdings Inc. Medpace is a full service clinical research organization(CRO)that provides Phase I-IV clinical development services to biotechnology, pharma ceutical, and medical device companies. Moreover, the company is known for making complex drug development process seamless through its global presence, scientific and medical expertise and full service delivery model with therapeutic focus. Medpace is also known for additional services like central laboratory, Bioanalytical and Imaging & ECG core Laboratories. Medpace’s unique global partnering concept places a strong emphasis on clinical research as well as the highest ethical standards and work performance. Its specialist teams work as an extension of their client’s teams, engaging promptly and providing strategic thinking to ensure faster startup times, greater quality, and the most efficient delivery of the clinical trial at every stage.
Dr. Kashid joined Medpace in 2018 with the aim to expand the team in the Asia Pacific region, particularly for clinical project management group. His role at Medpace is ranged from providing oversight on global clinical research projects for novel drugs in the Asia Pacific region, strengthening the team maintaining staff retention to assisting the company in expanding its business as well.“Our aim as the name indicates, is to bring medicine to market faster and more seamlessly, without adding complexity to the process” signifies Dr.Kashid.
Over the years, Medpace has spread its footprints across the globe in more than 40 countries and has been listed as America’s best midsize company in 2021 and 2022 by Forbes Magazine. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics by leveraging local regulatory and deep therapeutic expertise across all major areas, including oncology, cardiology, metabolic disease, endocrinology, central nervous system, and antiviral and anti-infective therapies. Dr. Kashid concludes “The clinical research future appears to be more dependent technology evaluation and adapting more patient centric approach by implementing decentralized trial solutions while maintaining traditional clinical trial management process to ensure regulatory compliance and patient safety. Further, real world data and blockchain technology will have a greater impact on future drug development , allowing for more efficiency and effective medicine to reach the market faster than in the past.”
The need to get new medicine in the market and helping mankind to live longer and healthier lives is the key aspect that drive dr. Pramod kashid towards the purpose
Dr. Kashid joined Medpace in 2018 with the aim to expand the team in the Asia Pacific region, particularly for clinical project management group. His role at Medpace is ranged from providing oversight on global clinical research projects for novel drugs in the Asia Pacific region, strengthening the team maintaining staff retention to assisting the company in expanding its business as well.“Our aim as the name indicates, is to bring medicine to market faster and more seamlessly, without adding complexity to the process” signifies Dr.Kashid.
Over the years, Medpace has spread its footprints across the globe in more than 40 countries and has been listed as America’s best midsize company in 2021 and 2022 by Forbes Magazine. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics by leveraging local regulatory and deep therapeutic expertise across all major areas, including oncology, cardiology, metabolic disease, endocrinology, central nervous system, and antiviral and anti-infective therapies. Dr. Kashid concludes “The clinical research future appears to be more dependent technology evaluation and adapting more patient centric approach by implementing decentralized trial solutions while maintaining traditional clinical trial management process to ensure regulatory compliance and patient safety. Further, real world data and blockchain technology will have a greater impact on future drug development , allowing for more efficiency and effective medicine to reach the market faster than in the past.”