Provides medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed
Attends and presents at investigator and sponsor meetings, provides medical consultation to clients, investigators and project team members and supports business development activities
Provides medical review and analysis for clinical trial serious adverse events, marketed products ICSR and periodic safety reports (e.g. PBRER, PSUR, DSUR) as well as other client deliverables
Requirements
MD or equivalent required
Active medical licensure preferred but not required
Candidates should have clinical experience in Nephrology and formal training in Nephrology (i.e residency and/or fellowship)
Patient treatment experience (comparable to 2+ years)
Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company or as a principal investigator (comparable to 1-2 years) in the industry
Direct experience in safety/Pharmacovigilance (comparable to 2 years)
Benefits
competitive remuneration
annual incentive plan bonus
healthcare
range of employee benefits
Applicant Tracking System Keywords
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