Samir Khoury M. D.

Experience

1. Senior Associate Director, Clinical Development Medical Affairs (Medical, Legal, Regulatory)

   Boehringer Ingelheim

   May 2015 — Present · Ridgefield, CT, US

   Review and evaluate the medical and scientific accuracy of promotional and non-promotional materials such as slide sets, sales aids, dossier updates, training materials and medical response letters. • Function as a key strategic partner with Legal, Regulatory, Marketing and Compliance to uphold standards and adhere to guidelines surrounding development and approval of materials. • Maintain a strong understanding of compliance standards and regulations governing the pharmaceutical industry surrounding creation and utilization of promotional and non-promotional materials. • Suggest revisions to material based upon accuracy, relevancy, and validity of supporting scientific evidence • Maintain a high level of awareness of relevant scientific literature and suggest appropriate sources of support for statements in promotional and non-promotional materials • Ensure all required revisions are made to materials prior to final approval and approve materials in a timely manner • Perform pre-review of materials to enable input at live, scheduled review meetings • Attend weekly, live committee meetings as the Medical representative • Stay current with new publications within therapeutic areas to be able to evaluate accuracy and balanced scientific representation of materials under review • Share new publications with Medical Affairs team to enable incorporation into medical response materials and educational content as appropriate • Help maintain literature database to facilitate the review process as time allows •Assist with other Medical Affairs projects and/or initiatives as required

Education

• CETEC University and Medical School Dominican

  Doctor, Medicine

• Westchester Community College Mercy College

  Pre-Medical Studies (Biology; Chemistry Psychology