Sandhiya Mohan
About Sandhiya Mohan
Sandhiya Mohan is a Senior Research Analyst specializing in clinical studies at Clarivate Analytics, with over eight years of experience in the field. She has a strong background in biotechnology and has previously worked at Thomson Reuters in various analytical roles.
Work at Thomson Reuters
Sandhiya Mohan has extensive experience at Thomson Reuters, where she worked in various roles over several years. She began her tenure as an Associate Analyst in Editorial Operations from 2007 to 2009. Following this, she served as a Research Analyst from 2009 to 2010. After a brief period away, she returned to Thomson Reuters as a Research Analyst-QC in 2010, where she has continued to work for 14 years in the Chennai Area, India. Her responsibilities have included cataloging and processing references from diverse scientific resources.
Current Role at Clarivate Analytics
Currently, Sandhiya Mohan holds the position of Senior Research Analyst-Clinical Studies at Clarivate Analytics, where she has been employed since 2016. Based in Bangalore, she has accumulated 8 years of experience in this role. Her work involves extracting critical data related to vaccines, drug discovery, and biomarkers from various scientific resources, including FDA regulatory documents and clinical trials. She also acts as a liaison for team members, assisting in updating process policies and manuals.
Education and Expertise
Sandhiya Mohan has a solid educational background in Biotechnology. She earned her Bachelor of Science (B.Sc.) degree from Periyar University, where she studied from 2002 to 2005. Following this, she pursued a Master of Science (M.Sc.) in Biotechnology at Bharathiar University from 2005 to 2007. Her academic training has equipped her with expertise in areas such as pharmacogenomics, toxicogenomics, and drug-gene expression, which are critical in her current research roles.
Background in Research and Analysis
Sandhiya Mohan has a strong background in research and analysis, particularly in the fields of clinical studies and scientific data extraction. Her experience includes cataloging and processing references from journals, meetings, reports, and series. She is skilled in tracking information related to adverse events and has a keen interest in roles that require continuous learning and skill development. Her analytical skills are complemented by her ability to collaborate effectively with team members.