Medical Reviewer/Safety Reviewer

Responsibilities include medical review, which involves in-house review of Case Report Forms (CRFs) including query resolution and addenda writing, QA of data listings. May manage the activities of regional contract CRAs, and organizes the files and budgets associated with several clinical studies. Provides medical support which may include: Adverse Event Reporting - the investigation and reporting of medical product experiences, in depth investigation of medical adverse events and works with Medical Affairs, Clinical, and Regulatory Affairs in the preparation of documentation on adverse events for the FDA; or Medical Communication which includes writing standard and custom responses to communication requests, in-depth assistance to the medical and lay community by responding to inquiries with medical/scientific information that is more complex and requires more data than is supplied in the package insert or the standard letter database. Off-label information would be disseminated at this level. May provide training internally and at investigator meetings on safety issues, responsible for serious adverse events and CRF completion, writing study summaries, and review protocols, study summary investigator brochures and IND annual updates for safety data verification. BS Perferred.

 

Motivated, self-starting, conscientious individual with a minimum of 2 years experience in pharmaceutical, clinical pharmacovigilence. Responsible for a high volume of SAEs--tracking, processing, and following up, within multiple clinical trial indications. Also, responsible for review and reconciliation of clinical data listings. MUST possess a medical background with related degree. We will also look at people with site coordinator experience with medical background. Must have extensive SAE review and follow up. BSN or RN's are preferred with safety experience.