Dr Gopi Adhvaryu

Multi-talented Dedicated clinical research professional proficient in complying with study protocols, standard operating procedures and good clinical practices, handling patient information and compliance procedures for different clinical trials. Well-organized and hardworking with excellent communication and planning skills. Practiced problem-solver with strong attention to detail. Prepared to offer 2+ years' experience in the field and take on a fast-paced position. Clear awareness of diverse backgrounds, alert to widely varied patient needs and circumstances, acting as a key resource to colleagues and allied health professionals.

• English
• Hindi
• Gujarati

• Gained exposure to research in; 1. EVALUATION OF PHARMACEUTICAL CARE IN DIABETIC PATIENTS IN COMMUNITY 2. STUDY OF ANTIBIOTIC PRESCRIPTION PATTERN AND ANTIBIOTIC SENSITIVITY IN SURGERY PATIENT IN TERTIARY CARE HOSPITAL. In each role, I earned commendations for the quality of my research, including data collection, quantitative analysis and results interpretation, paper preparation for presentation and publication.
• Poster presentation at the Professional Society for Health Economics and Outcomes Research (ISPOR) 6th Asia Pacific Conference, held in Beijing, China, "STUDY OF ANTIBIOTIC PRESCRIPTION PATTERN AND ANTIBIOTIC SENSITIVITY IN SURGERY PATIENT IN TERTIARY CARE HOSPITAL" was published in ISPOR's scientific journal, Value in Health, in Volume 17, Issue 7. Lalwani, T., Adhvaryu, G., Joshi, D., Deshpande, S. and Shah, G., 2014. Study of Antibiotic Prescription Pattern and Antibiotic Sensitivity in Surgery Patient in Tertiary Care Hospital. Value in Health, 17(7), p.A799.

->STUDENT VOLUNTEER AT ISPOR - SEPT 2014 

->CLINICAL RESEARCH PROFESSIONAL/CLINICAL RESEARCH COORDINATOR AT GOVERNMENT (CIVIL) HOSPITAL - JUNE2014 to JUNE 2016

• Identifying/selecting a principal investigator who will be responsible for the conduct of the trial at the trial site
• Setting up the trial sites (site management), which includes ensuring each center has the trial materials, including the trial drug often known as the investigational medicinal product, recruitment and retention issue identification and resolution
• Training the study staff (implementation, communication) in standard operating procedure for the clinical trials as per applicable regulatory requirements
• Verify that investigator and investigator's team are adequately trained and comply with the protocol, collaborated effectively with Research Coordinators, Research Nurses, and other Research Assistants in a team-based environment to facilitate the smooth execution of research studies
• Informed consent form review, case report form review, investigational drug accountability, and adverse event review, maintained strict confidentiality to keep personal information and collected data private
• Evaluated proof of eligibility and consent for participants
• Reviewed site regulatory binder to check collection procedures and completeness of paperwork,Providing support and assistance with various trial-related activities, contributing to the overall progress and success of the research endeavors.