Gemma Gills

Principal Clinical Research Associate @Medpace

London, GB
MOBILE NUMBERS
+91 *********19

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WORK HISTORY

Oct 2024 — Present

Principal Clinical Research Associate @Medpace

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Lead CRA• Conduct site qualification, initiation, monitoring, and close-out visits according to ICH-GCP, Medpace/Sponsor SOPs, and applicable regulatory requirements• Responsible for overall site management for assigned sites, including written and verbal communication and scheduling of monitoring visits• Responsible for the completion of visit reports, follow-up letters, and maintenance of study-related databases• Act as a resource and facilitate training for new CRAs

EDUCATION

N/A

Newcastle University

Master of Science (MS), Drug Chemistry

N/A

Newcastle University

Bachelor of Science (BS Hons), Chemistry

SKILLS

ScienceBiotechnologyData ManagementLife SciencesPharmaceutical IndustrySopElectronic Data Capture (Edc)Clinical Data ManagementRegulatory AffairsOncologyProtocolCROCancerGcpIch-GcpClinical MonitoringGood Clinical Practice (Gcp)EdcCtmsProject CoordinationClinical TrialsClinical ResearchClinical Development

ABOUT GEMMA GILLS

Experienced Clinical Research Associate with a demonstrated history of working in early phase oncology for a Contract Research Organisation. Skilled in Electronic Data Capture (EDC), Monitoring, Clinical Data Management, Good Clinical Practice (GCP), and Biotechnology. Strong research professional with a Master of Science (MSc) focused in Drug Chemistry from University of Newcastle-upon-Tyne.

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