Virtual Info Session for Nursing Professionals
Core
Transition clinical nursing knowledge into office-based corporate roles reviewing clinical trial data and managing patient safety events.
Role type
Clinical Data Review & Safety Coordination
Builds
Clinical trial data packages and safety reports for biotech/pharma clients
Domain
Clinical Research / Pharmacovigilance
Required skills
Clinical data review, Query resolution, Safety event tracking, Medical terminology, Regulatory knowledge, Therapeutic area specialization
Preferred skills
Pharmacovigilance experience, Oncology, Infectious Disease, Cardiology, Endocrine, Hematology
Responsibilities
Review clinical data collected in trials, Generate and resolve queries to clarify inconsistent clinical data, Collect, process, and track incoming adverse and serious adverse events, Write safety narratives, Report on various safety data, Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes
Seniority
Entry-level to Mid-level, structured growth
