Chayan Kumar Chakraborty

About Chayan Kumar Chakraborty

Current Responsibilities (Feb 2024 onwards): Clinical Research Associate 2 - Clinical Operations.More than 4.7 years’ experience in active monitoring of multinational and international Phase II, and IV clinical trials in Medical Oncology, Hematology, Immunology, Neurology, Pulmonology and Endocrinology indications.Associated Responsibilities (Oct 2022 - Jan 2024): Feasibility Team Lead 1. Feasibility Team Management - Managed 08 team members located in India.2. Develop blinded feasibility outreach database.3. Prepare Therapeutic Areas Presentation based on disease epidemiology & ongoing trials. Working closely with project leads for efficient site identification and start up.Previous experience (Apr 2018 to Jan 2021):1. Clinical Research Coordinator - Responsible for onsite planning, conducting, and summarizing all aspects of the study including identifying potential patient for study. Assisting the investigator in conducting the study as per the protocol, SOP, regulatory guidelines.2. Project Coordinator – Responsible for conducting health camp and awareness sessions on “Dengue Prevention, Awareness and Hand Washing Activities” in various schools, college, office, and resident welfare associations in this unprecedented public health intervention. Organized more than 100 camps in different district of Haryana and Delhi.General Summary of Experience:1. Handled at various stages in clinical study including Site Identification, Site Start up, Site Selection, Site Initiation, Site Monitoring and performing Site Closeout.2. Ensuring adherence to SOPs, ICH-GCP and GPP guidelines and other regulatory requirements.3. Tracking and follow up to procure study status, patient status, patient-visit status, study related documents, materials from sites.4. Knowledge and experience with various systems like CTMS, Infosario, Peoplesoft, MEDIDATA, DrugDev, Viedoc, Sitero, ALMAC, InfoLink etc.5. Assisting the Clinical project manager with follow up for project deliverables by collating updates from the others CRA\'s, training and mentoring new team members.6. Prepare and develop “Information, Education and Communication (IEC)” materials to convey public health messaging to community.7. Faced DCGI inspections for multiple sites for an Immunology study, with no critical or major observations, in the year 2023.8. Handled on an average, 06 sites in 07 protocol in Phase II and Phase studies in between the year 20••••25.

Experience

1. Clinical Research Associate 2

   IQVIA

   Feb 2024 — Present · Bengaluru, IN

Education

• Apeejay Stya University

  Master's degree

Skills

• Microsoft Excel
• Microsoft Powerpoint
• Microsoft Word
• Microsoft Office
• Leadership
• Research