Ruchi Bhavsar

Seeking a position to utilize my knowledge and abilities in medical research. that offers competitive environment, a true profession to put in the acquired knowledge of clinical trial protocol, and excellent communication abilities to support the efficient execution of clinical trials.

• GLP
• GCP
• GMP

• Assisted in the coordination and management of clinical trials in accordance with study protocol, regulatory requirements, and GCP guidelines.
• Prepared and maintained essential document including informed consent formed, case report forms and study binders.
• Supported the recruitment and screening process of potential study participants.
• Managed study related supplies, inventory and investigational products.
• Collaborated with study team members to ensure timely and accurate data collection, entry and reporting.
• Assisted in organizing and preparing for study related meetings, including investigator meetings and monitoring visit.
• Prepared and maintained study specific tracking tools, status reports, and study progress updates.
• Good command one TMF software also uploading all study related documents on daily basis.
• Managing data related to adverse events also life threating adverse events.
• Managing SQV SIV and SMV documents