Medical Director, Medical Affairs Certified Nephrologist

What you will do: Medically manages clinical trials to which s/he is assigned as MMServes as Global Lead MM (GLMM) for pan-regional and/or global trial(s) to which s/he is assigned Collaborates with the other members of the Medical & Safety project teams to process Serious Adverse Events (SAEs)Provides therapeutic and protocol-specific training to the project teams Contributes medical input into the design of clinical development programs, study protocols, research papers, client focused white papers, etc Provides after hours medical support for projects to which s/he is assigned What you will bring to the role Excellent computer skills (Word, Excel, Access)Excellent spoken and written English skills Excellent organizational and time management skills Excellent communication skills Excellent presentation skills Your experience Medical Degree from an accredited institution of Medical Education. At least 2 years of medical monitoring in clinical research or related industry Valid passport and ability to travel as required.