
Pharm.D graduate with specialized training in Clinical Research, Clinical Data Management, and Pharmacovigilance. Currently working as a Clinical Trial Data Analyst with experience in managing clinical data, supporting protocol compliance, and ensuring regulatory standards (ICH-GCP, FDA). Demonstrated capability in scientific communication, patient counseling, and engaging healthcare professionals. Passionate about oncology and medical affairs, with a strong foundation in evidence-based medicine, stakeholder collaboration, and therapeutic knowledge. Willing to travel extensively for field-based responsibilities.
Clinical Research & Medical Affairs
Scientific Communication & Stakeholder Engagement
Clinical Trial Monitoring & Data Validation
Pharmacovigilance & Regulatory Compliance
EDC Systems: Medidata, Oracle InForm
UAT Testing & Process Improvement
Microsoft Excel, Office, SQL (basic)
Strong Verbal & Written Communication
Attention to Detail & Problem Solving
Advanced Diploma in Clinical Research, CDM, and Pharmacovigilance – Cavaxion Clinical Research Institute