Dr. Vaibhav Bari

Clinical Trial Assistant|Clinical research

• Contributed to clinical trial activities involving multiple drugs across different therapeutic areas.
• Gained practical exposure to clinical research processes, clinical trial coordination and study documentation.
• Developed an understanding of Good Clinical Practice (GCP), research ethics, clinical trial protocols and patient safety principles.
• Acquired foundational knowledge of drug development, clinical trial conduct and the importance of data quality and regulatory compliance.

Pharmacovigilance |Drug Safety and Clinical Research.

• Developed an understanding of pharmacovigilance principles, adverse drug reaction (ADR) monitoring, and drug safety assessment.
• Familiar with the identification, documentation, and reporting of adverse events, and suspected adverse drug reactions in clinical research settings.
• Acquired knowledge of drug safety surveillance throughout the clinical development and post-marketing phases of the drug lifecycle.
• Familiar with the principles of Good Clinical Practice (GCP), patient safety monitoring and ethical conduct of clinical trials.
• Developed foundational knowledge of benefit–risk assessment, medication safety and the importance of accurate safety documentation.

General Secretary,|Sion MARD, LTMMC & GH, Mumbai

• Coordinated resident-doctor association activities, facilitating communication between resident doctors, hospital administration, and institutional authorities to address residents’ concerns.
• Led administrative coordination, official correspondence, meeting documentation, and implementation of committee decisions to ensure effective organizational functioning.
• Organized healthcare initiatives, including HPV vaccination and blood donation drives, promote preventive healthcare and community health awareness.
• Represented resident doctors in advocacy initiatives concerning welfare, working conditions, and stipend-related issues, while collaborating with stakeholders to facilitate constructive resolutions.

Medical Affairs Intern| Abbott

• Completed a structured internship program with exposure to Medical Affairs and RMA (Regional Medical Affairs/Medical Representative Affairs, depending on the organization's terminology) functions.
• Gained insights into medical strategy, scientific communication, and evidence-based product information within the pharmaceutical industry.
• Collaborated with Medical Affairs team members to understand medical information dissemination, scientific engagement, and cross-functional coordination.
• Developed an understanding of pharmaceutical industry practices, medical compliance and the role of scientific evidence in supporting clinical decision-making.