Alexandra Rivers Email & Phone Number

Loughton, Gb

London Area, United Kingdom

- Responsible for data entry and query resolution in a range of EDC systems, including iMedidata, InForm, TrialMaster, and several academically owned databases.- Currently managing ten first-in-human- and early-phase, industry, and non-commercial oncology trials as the primary data lead.- Principal overseer of ISF maintenance, which includes the collection, review, and filing of essential site documentation, to ensure continual inspection-readiness of site.- Responsible for case report form curation.- Key liaison between the multi-disciplinary site team, CRO, sponsor, and third-party vendors for day-to-day site activities.- Principle delegate for all monitoring activities at site, including MHRA inspections and sponsor audits.- Primary coordinator for trial close-out tasks. - Accountable for the accurate and timely reporting of AEs and SAEs according to GCP and protocol-specific guidelines.- Responsible for the training and support of staff in clinical study systems and procedures.- Integral in the coordination of team meetings.

Drug Development Science Msc, Distinction

Modules: - Preclinical Science - 81% - Clinical Drug Development - 77% - Advanced Clinical Pharmacology - 76% - Drug Safety and Ethics.

Bachelor'S Degree, Biochemistry, First Class