Sharmila Kumar
About Sharmila Kumar
Sharmila Kumar is a Clinical Trial Monitor - CRA II at Bristol-Myers Squibb with extensive experience in oncology clinical trials and a background in pharmaceutical science and biomedical science.
Company
Sharmila Kumar currently works at Bristol-Myers Squibb as a Clinical Trial Monitor - CRA II. She rejoined the company in her current role after a previous stint as a Clinical Trials Associate from 2015 to 2016. Her responsibilities include overseeing clinical trials, ensuring compliance with protocols, and collaborating with various stakeholders.
Title
Sharmila Kumar holds the title of Clinical Trial Monitor - CRA II at Bristol-Myers Squibb. In this role, she leverages her extensive experience in clinical trial monitoring, specifically in oncology, to oversee study sites and ensure protocol compliance.
Education and Expertise
Sharmila Kumar earned a Bachelor of Biomedical Science degree from RMIT University from 2011 to 2014, specializing in Pharmaceutical Science. She also holds a Bachelor of Science (BS) in Statistics from La Trobe University, achieved between 2006 and 2008. Kumar's education is complemented by her VCE from Mentone Girls Secondary College, attained from 2003 to 2005. Her expertise includes monitoring clinical trials in oncology, particularly in Melanoma, RCC, and NSCLC, and training site personnel on protocols and regulatory requirements.
Background
Sharmila Kumar's career spans various roles in the healthcare and pharmaceutical sectors. She has held positions including Clopine Services Coordinator at Hospira, Clinical Trials Associate at Bristol-Myers Squibb, and Clinical Research Associate II at Syneos Health. Additionally, she has experience as a Clinical Trial Assistant at GSK and as a Pharmacy Assistant at Baileys Pharmacy and Your Pharmacy. Her diverse work history underscores her comprehensive understanding and experience in clinical trials and pharmaceutical services.
Achievements
In her role as Clinical Trial Monitor - CRA II, Sharmila Kumar acts as a Lead Site Monitor collaborating closely with Clinical Site Managers, Field Medical, and Protocol Managers. She ensures the safety and protection of study subjects, adheres to monitoring plans, SOPs, ICH/GCP Guidelines, and local regulations, and supervises site personnel without direct authority. Her ability to influence site personnel and identify opportunities to build professional relationships significantly contributes to the successful achievement of study objectives.