Risha Chavda
About Risha Chavda
Risha Chavda is the Manager of Clinical Trial Associates & Contract Administrators at Bristol-Myers Squibb in Uxbridge, UK, with over a decade of experience at the company and extensive background in clinical data management.
Current Role at Bristol-Myers Squibb
Risha Chavda is currently employed as the Manager of Clinical Trial Associates and Contract Administrators at Bristol-Myers Squibb located in Uxbridge, UK. She has been with the company since October 2011, showcasing a long-term commitment and extensive experience in the pharmaceutical industry. This role emphasizes her capability in overseeing clinical trial operations as well as contract administration.
Previous Positions at Bristol-Myers Squibb Pharmaceuticals
From 2007 to 2011, Risha Chavda worked at Bristol-Myers Squibb Pharmaceuticals in Singapore as an Interim Manager and Clinical Data Quality Manager. Over four years, she accumulated valuable experience managing clinical data quality, contributing to her robust understanding of data integrity and accuracy in clinical trials.
Experience at SRG UK
Risha Chavda held the position of Team Leader, Phase I, Clinical Data Management at SRG UK from 2006 to 2007. During her one-year tenure, she led teams in managing clinical data for Phase I trials, gaining hands-on experience in the early stages of clinical trial data management.
Tenure at PAREXEL International
Risha Chavda worked at PAREXEL International for nine years, from 1997 to 2006, where she held the role of Team Leader, Data Management. This long duration highlights her strong foundation in data management practices and leadership in clinical operations. Her role involved overseeing data-related activities, ensuring that data collection and processing met rigorous industry standards.
International Experience
Risha Chavda has extensive international work experience, including a significant tenure in Singapore before her current role in the UK. Her global exposure has provided her with diverse perspectives and practices in clinical data management and clinical trials, enhancing her ability to manage and lead teams across different cultural and regulatory environments.