Angana Roy

As a dedicated and enthusiastic job seeker with strong skills in communication, self-management, clinical research, and clinical data management, I am keen to join a team that values innovation and excellence in clinical research and data management. I am ready to use my education, experience, and competencies to support the goals of the organization and learn from the best in the field.

• Basics of Clinical Trials including definitions, importance, benefits, possible risks.
• Importance of Clinical research in Drug discovery and development
• Phases of Clinical Research
• 13 principles of ICH-GCP
• Roles and responsibilities of Sponsor, CRA, CRC and PI
• General knowhow about preparation of key documents in Clinical Research like ICD, IB, CRF, CSR, etc.
• Knowledge about objective, content and preparation of Clinical Trail Protocol.
• Importance of Drug safety reporting and Drug accountability
• Knowledge about rules and regulations of conducting Clinical trails in India as per NDCT 2019

• Importance and basics of Clinical Data Management, process flows and tools
• Process of Clinical data management plan and Data Validation
• Knowledge about Design and contents of Case Report Form (CRF) with CRF completion guidelines
• Perform Data Entry to transform data fro CRF to Data Management system database
• Basic understanding of quality control processes like discrepancy or query management
• Idea about Medical coding process of classifying reported events and SAE reconciliation
• Basic understanding of Electronic Trail Master File (eTMF)
• Understanding about Data Integrity (ALCOA + 2 CEA principle)

Completed project work - 'Effects of heavy metals (Lead) on the morphology of some Gregarine parasite from Earthworm (Lampito sp.)'

Web designing certification

• Travelling
• Listening Music
• Cooking