Academic Calendar-B. Pharm. & M. Pharm. 2026-2027 Click here M.Pharm. Vacant Quota Seats Admission 2026-27 Click here
Academic Calendar-B. Pharm. & M. Pharm. 2026-2027 Click here M.Pharm. Vacant Quota Seats Admission 2026-27 Click here
Ms. Mansi Patel
Education Qualification
M.Pharm ( Pharmacology )
Designation
Department
Research Area
· Clinical Research and Clinical Trial Coordination
· Clinical Documentation and Regulatory Compliance
· Pharmacology and Preclinical Research
· Pharmacovigilance and Drug Safety
· Quality Assurance and Clinical Data Management
General Information
· Completed B.Pharm (CGPA 8.60/10) and M.Pharm in Pharmacology (CGPA 9.20/10) from Shree S. K. Patel College of Pharmaceutical Education & Research, Ganpat University.
· Worked as Clinical Research Coordinator Intern at Cytex Clinical SMO (July 2025–February 2026).
· Experienced in clinical trial documentation including CRF, ICF, protocol and screening forms.
· Knowledge of in-vivo experimental models, animal handling, dosing, sample collection and observation.
· Understanding of GCP, ICH-GCP guidelines, Schedule Y and regulatory requirements.
· Strong communication, literature review, scientific writing and clinical data management skills.
· Completed workshops on Skill Enhancement for Dosage Form Development, HERO'S Impact from Clinical Trials to Patient Access and Good Clinical Practice (NIDA Clinical Trials Network).
· Areas of interest include Clinical Research, Clinical Trial Management, Pharmacovigilance, Regulatory Affairs, QA/QC and Clinical Documentation.
Profile
General Information
Ms. Mansi Patel has completed her M.Pharm in Pharmacology from Shree S. K. Patel College of Pharmaceutical Education and Research, Ganpat University. She has academic training in pharmacology, preclinical screening, drug mechanisms and clinical research. She worked as a Clinical Research Coordinator Intern at Cytex Clinical SMO where she supported patient screening, informed consent, study documentation, investigator coordination and regulatory file management. She has knowledge of ICH-GCP guidelines, Schedule Y, clinical trial documentation and basic regulatory submissions.