Yadav Patil
Clinical research
Talent
PuneMember since April 3, 2026
ICH-GCP GuidelinesClinical Trial Phases (I–IV)Case Report Forms (CRF)Trial Master File (TMF)Adverse Event (AE/SAE) ReportingSource Data Verification (SDV)Protocol ComplianceClinical Data ManagementMS ExcelMS WordPowerPointClinical Data Management SystemsDocumentation & Record KeepingAttention to DetailCommunication SkillsTeam CollaborationTime Management
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ICH-GCP GuidelinesClinical Trial Phases (I–IV)Case Report Forms (CRF)Trial Master File (TMF)Adverse Event (AE/SAE) Reporting
About
Detail-oriented B.Pharm graduate with strong knowledge of ICH-GCP, clinical trial processes, and regulatory documentation. Seeking a Clinical Research Associate (CRA) or Clinical Trial Assistant (CTA) role to support clinical trials, ensure protocol compliance, and contribute to accurate data management. Open to relocation and immediate joining.
Experience
Production Trainee at Emcure Pharmaceuticals Ltd.
Trainee role supporting pharmaceutical production and quality assurance operations with focus on GMP compliance and regulatory documentation.
- Maintained and reviewed Batch Manufacturing Records (BMR) ensuring GMP compliance
- Collaborated with QA/QC teams to support audits and regulatory inspections
- Followed SOPs and ensured adherence to regulatory guidelines
- Assisted in deviation reporting and CAPA processes
- Strengthened documentation practices aligned with clinical research standards
Education
Bachelor of Pharmacy in Pharmacy – SRTM University, Nanded
Skills
Clinical research
