Summary
The Fountain Group is a national staffing firm and we are currently seeking a Pharmacovigilance Manager for a prominent clientof ours. This position is Remote. Details for the position are as follows:Job Description:Details:Pay for this position is 100.00 to 121.15 hourly depending on experience.This position is a one year contract with the possibility of extension or conversion to permanent.Requirements: Minimum 7 years Pharmacovigilance experience, including experience in aggregate safety reports and safety signal management.Bachelor's Degree in biologic or natural science; or health case discipline. Advanced degree (PhD, MPH, NP, PharmD, etc.) preferred.Responsibilities: Leads the signal management process (i.e., signal detection, signal tracking, signal documentation, facilitating decisions regarding signals and safety risk, etc.) for assigned product(s) and evaluates safety data and signals as part of ongoing pharmacovigilance activities.Includes synthesis of data from multiple sources and authoring signal evaluation reports.Leads signaling review process and product Safety Signaling Team meetings.Manages literature review for safety information.Leads and conducts, independently and/or collaboratively, all aspects of substantive projects such as signaling, authoring of aggregate data reports, and responses to regulatory agency requests.#J-18808-Ljbffr
Job Description
The Fountain Group is a national staffing firm and we are currently seeking a Pharmacovigilance Manager for a prominent clientof ours. This position is Remote. Details for the position are as follows:Job Description:Details:Pay for this position is 100.00 to 121.15 hourly depending on experience.This position is a one year contract with the possibility of extension or conversion to permanent.Requirements: Minimum 7 years Pharmacovigilance experience, including experience in aggregate safety reports and safety signal management.Bachelor's Degree in biologic or natural science; or health case discipline. Advanced degree (PhD, MPH, NP, PharmD, etc.) preferred.Responsibilities: Leads the signal management process (i.e., signal detection, signal tracking, signal documentation, facilitating decisions regarding signals and safety risk, etc.) for assigned product(s) and evaluates safety data and signals as part of ongoing pharmacovigilance activities.Includes synthesis of data from multiple sources and authoring signal evaluation reports.Leads signaling review process and product Safety Signaling Team meetings.Manages literature review for safety information.Leads and conducts, independently and/or collaboratively, all aspects of substantive projects such as signaling, authoring of aggregate data reports, and responses to regulatory agency requests.#J-18808-Ljbffr
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