Verified recordProfessional Services

Chike Dellimore

Pv Consultant Pharmacovigilance, Risk Management and Safety Surveillance at Eliquent Life Sciences

Based in Charlottesville, United States

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Seniority

Manager

Department

Healthcare & Human Services

Location

Charlottesville

Industry

Professional Services

Company size

570

Contact information

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Email

1 credit

c•••••••@eliquent.com

Phone

5 credits

+1 ••• •••• ••••

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Background

About Chike Dellimore

Global Drug Safety Expert with 18+ years of experience in clinical research and pharmacovigilance (PV). Expertise with Phase 1 – 4 studies in multiple therapeutic areas. Strong PV audit, root cause analyses, and process documentation skills. Adept at knowledge gap analyses, including action plan identification, implementation, monitoring and evaluation. Developed, updated, and delivered PV training content to a global safety team. Excellent cross-functional collaboration, stakeholder relationship management, and people leadership abilities. US Citizen; Fluent in English (Native speaker). THERAPEUTIC AREAS Autoimmune Disorders, Hematology, Internal Medicine, Gastroenterology, Neurology, Oncology DOCUMENTATION Standard Operating Procedures (SOPs), Work Instructions (WIs), Guidance Documents, Templates, CAPA Plans, Safety Management Plans, Reconciliation Plans, Literature Search Plans, Individual Case Safety Reports DATABASE SKILLS Oracle ARGUS Safety Database, ARISg, MediData RAVE EDC System, DistillerSR COMPLIANCE Regulatory Reporting, FDA, EMA, ICH GCP, Institutional Review Boards (IRB), Ethics Committees (ECs), Development Safety Update Reports (DSURs), Executive Summaries, Analysis of Similar Events (AOSE), Sponsor audits and Regulatory inspections

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