Drug Safety Physician III

Title: Drug Safety Physician III Location: Danbury, CT Duration: 12 Months Responsibilities • Must have experience with review and interpretation of aggregate data, signal management, and optimally with authoring regulatory responses and PV-related documents for NDA submissions. • In addition to reviewing and interpreting aggregate data, may be responsible for assessing individual clinical trial and spontaneous case reports for medical review and determining regulatory reporting responsibilities; assessing seriousness, expectedness and causality; and querying for additional medical information needed to understand the event and determine causality Requirements: • Skills: MEDICAL CLEARANCES - Experience with complex PV analyses and authoring PV-related regulatory documents required • INDUSTRY EXP: Five years industry pharmacovigilance/risk mgmt and aggregate analysis of safety data Clinical Medicine experience with more than one year of patient care. Excellent written & verbal communication skills • Must have MD / DO and Medical license (US or equivalent) plus at least 1 year post license clinical experience. • Skills: MEDICAL CLEARANCES - Experience with complex PV analyses and authoring PV-related regulatory documents required • INDUSTRY EXP: Five years industry pharmacovigilance/risk mgmt and aggregate analysis of safety data Clinical Medicine experience with more than one year of patient care. Excellent written & verbal communication skills • Must have MD / DO and Medical license (US or equivalent) plus at least 1 year post license clinical experience. This Job is with one of my pharmaceutical client. Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at .