Sagarika Dhamne
Process Coordinator @IQVIA
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WORK HISTORY
Process Coordinator @IQVIA
Maintained and managed eTMF systems by performing QC, functional checks, EDL correction, following up with CRAs, ensuring timely filing, and checklist reconciliation. Conducted quality reviews of investigator documentation to ensure compliance with GCP and regulatory standards. Reviewed and quality-checked peer CTA tasks, supporting consistency, accuracy, and adherence to process requirements. Supported study teams and CRAs across all study phases (start-up, maintenance, close-out) with planning, milestone tracking, compliance checks, and clinical systems updates. Performed monitoring plan interval reviews to confirm visit schedules were met in accordance with study requirements. Handled user access management by maintaining study team lists, system role reviews, and permissions throughout the study lifecycle. Acted as SME/mentor for new joiners, supporting system/process trainings, guiding teams with system usage, creating/updating guidance documents, and relaying new updates. Provided administrative and operational support, including welcome communications, training assignment/withdrawal, audit/inspection readiness, and documentation follow-up.
EDUCATION
AISSMS College of Engineering
Bachelor of Pharmacy
Bharati Vidyapeeth College of Engineering, Navi Mumbai
Master of Pharmacy, Pharmacology
Bharati vidyapeeth college of Pharmacy
Master's degree, Pharmacology
St. Lawrence High School
High School Diploma
KRT Arts, BH Commerce and AM Science (KTHM) College, Nashik
High School Diploma
AISSMS College of Pharmacy - India
Bachelor's degree, Pharmacy
ABOUT SAGARIKA DHAMNE
Hi, i am Sagarika Dhamne works as clinical trial coordinator in IQVIA. I’m a dedicated clinical operations professional with hands-on experience supporting end-to-end study delivery — from planning and start-up to maintenance and close-out. Collaborating closely with SGTMs and C-CRAs, I ensure studies progress smoothly by driving efficiency, accuracy, and regulatory compliance across all phases.I’ve built expertise in study documentation management, milestone tracking, compliance oversight, access control, and clinical systems maintenance. I take ownership of creating reports, managing study metrics, coordinating training activities, and supporting eTMF and EDL processes to maintain data integrity and operational excellence.Beyond daily execution, I focus on optimizing workflows, strengthening cross-functional collaboration, and identifying process improvements that enhance quality and speed. I’m passionate about contributing to high-performing teams, learning continuously, and taking on responsibilities that drive both project success and personal growth.As I advance in my career, I aim to further develop my leadership and strategic skills to take on broader roles in clinical operations and project management — contributing to efficient, patient-focused clinical delivery.
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