This Assoc./ Medical Director role will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials.
Serve as a medical expert during project delivery life-cycle. Provide therapeutic medical and strategic expertise to business development activities.
RESPONSIBILITIES:The role includes predominantly Medical Monitoring responsibilities and Medical Strategic inputs as requested.
Medical Monitoring:Serves as Global and Regional Medical Advisor on assigned projects.Serves as Scientific Advisor and provides guidance to Project Leaders on the medical and scientific aspects of assigned projects.Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility.Performs medical review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs).Performs review and clarification of trial-related Adverse Events (AEs).REQUIREMENTS:Excellent communication, presentation and interpersonal skills, including the command of English language (both written and spoken).Medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education.Certification in Neurology (mandatory)3 - 5 years of prior relevant experience in general clinical medicine.Previous clinical research experience as an investigator or in the Pharma, CRO, or Biotech industry is required; or equivalent combination of education, training and experience.Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research.Excellent skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility.
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