A company is looking for a Veterinary Clinical Medical Monitor.
Key Responsibilities
Collaborate with clinical study teams to provide quality review over study data and monitor studies for regulatory approval of new animal products
Review Adverse Events (AEs) in clinical studies and assist in reporting Serious Adverse Events (SAEs) to Regulatory Affairs / Pharmacovigilance
Assist in authoring and reviewing Final Study Reports (FSRs) and ensure quality and compliance of raw data
Required Qualifications
Doctor of Veterinary Medicine with several years of practice experience (no active license required)
Clinical trial experience highly preferred
Experience with AEs / SAEs / PV / Regulatory affairs for safety monitoring preferred
Knowledge of Good Clinical Practice (GCP)
Medical Monitor • Des Moines, Iowa, United States