Medical Director

Contact: Jesse Klein
Phone: 215-830-9211 x126

Job Responsibilities:

  • Contribute to the training, leadership and continuing education for all of Clinical R&D.
  • Provide medical and scientific direction on clinical matters affecting preparation and submission of timely and sound information to the global regulatory agencies
  • Review all reported adverse events in clinical trials of investigational products. Assess, query and recommend corrections to MedDRA coding of adverse events. Approve MedDRA coding of adverse events
  • Provide strategic leadership to the department activities related to the evaluation and reporting of issues and adverse events related to products safety and efficacy, as well as strategies and activities associated with technical support for divisional products in the global clinical market
  • Participate in the development and writing of Clinical Trial Protocols. Provide input to investigator’s brochure and interim/final CSR’s. Approve final clinical trial protocols, investigator’s brochures and clinical study reports
  • Maintain knowledge base as to developments and trends in medical science pertaining to his/her area of responsibility
  • Work with product development and marketing functions to define the requirements and specifications for new products

Job Requirements:

  • Medical Doctorate (M.D.) degree with medical licensure in at least one state, and board certification
  • Ability to adapt and drive constant change is a critical attribute
  • At least 3-5 years of active medical or academic practice in the therapeutic area
  • At least 3-5 years relevant experience in the pharmaceutical/biopharmaceutical industry
  • Medical Doctorate (M.D.) degree referred
  • Excellent communication skills
  • Excellent oral and written communication skills (at least one major international language is preferred)

If interested, please send a MS Word version of your resume to Jesse Klein at


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