Innovative global pharma in Chicago area seeks senior level safety MD
Our client, a leading global pharmaceutical company, is looking for a senior-level industry MD to be based in Chicago, IL as a senior medical director, product safety and pharmacovigilance. This is a crucial position with a company that has a track record of explosive growth.
If you are a drug safety MD and would like to enhance your career, please email a Word document of your resume to afiore@kleinhersh.com If this opportunity does not match your interest, we have a number of additional roles that could work for you.
Responsibilities:
Responsible for leading and overseeing the Pharmacovigilance department to ensure effective systems for safety monitoring, assessment and reporting for investigational and commercialized pharmaceuticals. The responsibilities include data intake, handling and management for adverse events and medication errors; safety evaluation and analysis; risk assessment and management; and reporting to regulatory authorities in the US and Canada. Collaborates cross functionally and globally as needed to address findings, evaluate medical and business risk and recommend actions. Responsible for proactive awareness of regulatory and industry trends and direct interface with regulatory authorities.
Our client, a leading global pharmaceutical company, is looking for a senior-level industry MD to be based in Chicago, IL as a senior medical director, product safety and pharmacovigilance. This is a crucial position with a company that has a track record of explosive growth.
If you are a drug safety MD and would like to enhance your career, please email a Word document of your resume to afiore@kleinhersh.com If this opportunity does not match your interest, we have a number of additional roles that could work for you.
Responsibilities:
Responsible for leading and overseeing the Pharmacovigilance department to ensure effective systems for safety monitoring, assessment and reporting for investigational and commercialized pharmaceuticals. The responsibilities include data intake, handling and management for adverse events and medication errors; safety evaluation and analysis; risk assessment and management; and reporting to regulatory authorities in the US and Canada. Collaborates cross functionally and globally as needed to address findings, evaluate medical and business risk and recommend actions. Responsible for proactive awareness of regulatory and industry trends and direct interface with regulatory authorities.