Sr. Drug Safety Associate

DRUG SAFETY CONSULTANT 6 months+ Fully remote                                                        Our client is an emerging, mission-driven, drug development company intentionally designed to identify, clinical evaluate, and successfully commercialize novel treatments for pediatric oncology patients, and ultimately to expand those benefits to patients of all ages.                                                                                       RESPONSIBLITIES:   ·       As a Drug Safety Consultant, you will be expected to perform case processing for serious adverse events, serious and non-serious adverse drug reactions and other medically-related project information such as adverse events of special interest and clinical endpoints. ·       Complete QC of vendor cases to ensure quality levels are maintained per DOB’s expectations. ·       Management of the safety intake mailbox ·       Support the team as needed to ensure patient safety is monitored and maintained at DOB ·         REQUIREMENTS:   ·       Relevant clinical research/pharmaceutical industry experience, preferably in pharmacovigilance/drug safety – ARGUS global safety database, with knowledge of medical terminology and coding systems. ·       Must be fluent in written and verbal English with good communication skills and basic computer skills. Detail orientated and capable of working effectively within a team environment. ·       Medical/science background (nursing preferred) and/or bachelor’s degree or local equivalent.   The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification.   COMPENSATION   The hourly range for this $65/hour.