Revati Kamble
@revatikamble
Clinical research coordinator at Zenith Clinical Services who managed trial documentation, eCRF data, and regulatory submissions.
IndiaWhat I'm looking for
At Zenith Clinical Services, I supported clinical trials from the initial phase through conduct and closeout, following study protocols, ICH-GCP, NDCT rules, and site SOPs. I prepared essential and regulatory documents, entered eCRF data, and managed discrepancies.
As a Claims Processing specialist at Iassist Innovation labs, I review medical claims and analyze claim data for discrepancies. I also test claims software workflows and perform data entry and initial quality control for itemized medical bills.
Experience
Work history, roles, and key accomplishments
Claims Processing Specialist
Iassist Innovation Labs
Apr 2025 - Present (1 year 6 months)
Processed and reviewed medical claims with high accuracy, managed high-volume electronic claims, and conducted POC testing for claims software.
Trainee Clinical Research Coordinator
Zenith Clinical Services
Sep 2024 - Feb 2025 (5 months)
Executed clinical trials in accordance with ICH GCP and study protocols, managed essential documents, and ensured regulatory compliance.
Education
Degrees, certifications, and relevant coursework
Mangalore University
Master of Science, Microbiology
2018 - 2020
Completed M.Sc. in Microbiology from Mangalore University.
Raja Lakhamagouda Science Institute
Bachelor of Science, Chemistry, Botany, and Zoology
2015 - 2018
Completed B.Sc. with Chemistry, Botany, and Zoology from Raja Lakhamagouda Science Institute.
NIDA Clinical Trial Network
GCP Certification, Clinical Research
Earned GCP Certification from NIDA Clinical Trial Network.
Tech stack
Software and tools used professionally
Availability
Location
IndiaAuthorized to work in
Salary expectations
Job categories
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