

Doctor of Pharmacy (Pharm D) graduate with practical experience in clinical pharmacy, pharmacovigilance, and patient safety gained through internships and clinical clerkships. Possess strong interest in clinical research, oncology studies, and clinical trial operations. Knowledgeable in ICH-GCP principles, informed consent process, clinical documentation, medical data review, and adverse event monitoring. Experienced in multidisciplinary collaboration, laboratory data interpretation, and medication safety initiatives with excellent written and verbal communication skills.
Reviewed patient medical records, laboratory parameters, and medication histories to support evidence-based clinical decisions.
Participated in multidisciplinary ward rounds and collaborated with physicians, healthcare professionals, and other staff regarding patient management.
Assisted in medication safety initiatives and adverse event monitoring activities.
Maintained accurate clinical documentation and patient records.
Developed strong communication skills through interaction with patients and healthcare stakeholders.
Clinical Research
Clinical Trial Operations
ICH-GCP Guidelines
Medical Data Review
Clinical Documentation
Pharmacovigilance
Adverse Event Reporting
Informed Consent Process
Source Data Verification
Query Resolution
Regulatory Compliance
Data Collection
Stakeholder Communication
Laboratory Data Interpretation
Oncology Research
English Communication Skills
Interprofessional collaboration
Teamwork orientation
Medication reconciliation
Medication management
Merit level performance in national level mock test on Clinical research related domains