Gayatri More
Clinical Research Coordinator @Medicosurg Solutions Business Development
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WORK HISTORY
Clinical Research Coordinator @Medicosurg Solutions Business Development
Ahmedabad, IN
Assisting in conduct clinical trials as per ICH-GCP and regulatory standards- Supporting patient recruitment, screening, informed consent, and study visit coordination- Managing site initiation, monitoring support, and close-out documentation activities- Maintaining and updating Investigator Site File (ISF) and essential trial documents- Performing accurate source documentation and eCRF entry in Codengelo EDC- Handling EDC query resolution and protocol compliance tracking- Supporting AE/SAE documentation, reporting, and EC submission activities.
EDUCATION
Srinath college of pharmacy, Chh.Sambhajinagar, Maharashtra
Bachelor's degree, Pharmacy
ABOUT GAYATRI MORE
Welcome to my profile! I’m Gayatri More, a Clinical Research Coordinator (CRC) with a B. Pharmacy background and strong hands-on experience in clinical trial coordination, data handling, and regulatory-compliant documentation.I currently work on clinical studies, where I support day-to-day site operations including patient screening and informed consent, source documentation, CRF completion, EDC data entry, query resolution, and protocol adherence in compliance with ICH-GCP guidelines. I closely collaborate with investigators, site teams, and sponsors to ensure data accuracy, patient safety, and inspection-ready documentation.In addition to my CRC role, I hold advanced certifications in Clinical Research, Clinical Data Management, Pharmacovigilance, Medical Writing, and Regulatory Affairs, with practical internship exposure at ODCET Technologies and CliniWings Clinical Research. My experience includes ICSR case processing, MedRA coading, Narrative writing, Case Processing, Argus database, literature screening, CRF design, protocol review, and CTD, eCTD submission support, strengthening my understanding of the end-to-end clinical research lifecycle.I am now actively seeking opportunities in:Clinical Research • Clinical Data Management • Pharmacovigilance • Regulatory AffairsI bring strong attention to detail, regulatory knowledge, clear documentation skills, and a proactive mindset, with the ability to adapt and grow in fast-paced clinical and healthcare environments.Let’s connect if you’re looking for a motivated and well-prepared professional ready to contribute to high-quality clinical research and data integrity. Contact: g••••••••@gmail.com |+91••••••••05
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