Ahmedabad, Gujarat, India
PharmD graduate with experience in Clinical Research, Clinical Trial Operations, Medical Writing, and Healthcare Communication. I bring foundational exposure to clinical trial documentation, regulatory compliance, site coordination, and evidence-based scientific communication through my experience as a Clinical Trial Assistant (CTA) and healthcare professional. My experience includes supporting clinical documentation processes, publication activities, medical content development, and collaborative coordination with healthcare teams while ensuring accuracy, compliance, and adherence to clinical guidelines and GCP standards. During internships at Zydus Lifesciences and HCG Hospitals, I gained hands-on exposure to antimicrobial stewardship, patient counseling, clinical audits, and patient safety initiatives, strengthening my understanding of healthcare operations and clinical practices. Key competencies include: • Clinical trial documentation and coordination • GCP and regulatory compliance awareness • Medical writing and scientific communication • Site communication and stakeholder coordination • Clinical audits and patient safety initiatives • Publication and presentation support • Attention to detail and documentation management I am highly adaptable, detail-oriented, and passionate about building a long-term career in Clinical Research and Clinical Operations, with strong interest in CRA roles and global clinical development opportunities.
-Assisting in the preparation and maintenance of Site Investigator File (SIF) and electronic Trial Master File (eTMF) -Supporting the preparation and submission of Ethics Committee (EC) dossiers -Coordinating trial documentation and tracking study progress -Ensuring compliance with GCP, ICH, and regulatory requirements -Gaining hands-on experience in clinical trial operations and document management
- Actively participated in antimicrobial stewardship, optimizing antibiotic selection, dosage, and administration to reduce resistance - Conducted narcotic audits, ensuring controlled drug compliance, accurate documentation, and safe handling - Performed adverse drug reaction (ADR) monitoring and reported findings to the medical team. - Provided drug information support with evidence-based recommendations. -Assisted in pharmacy inventory management, ensuring availability and record accuracy. 👉 This internship strengthened my clinical decision-making, patient safety focus, and regulatory compliance skills.
I have worked at HCG hospital as a Clinical pharmacist intern and learned a lot during my tenure.