Clinical Research Physician - Global Pharmaceutical Firm

• An opportunity to work with one of the world’s largest pharmaceutical company
• An opportunity to independently handle all scientifc affairs for the portfolio

Our client is a global pharmaceutical giant.

The primary responsibility of the Medical Affairs CRP is to provide expert medical support to all aspects of the local business, to ultimately enhance the customer’s experience in interacting with the company. This includes local marketed product support (participate in the development of the "patient journey" and the strategic plan for the compound), medical support for regulatory affairs and interactions with government agencies (medical support for New and Supplemental New Drug Submissions and participating and presenting at meetings with government regulatory agencies), medical support for pricing, reimbursement and access(PRA) (providing medical guidance on the PRA plan and interacting with government PRA agencies as needed), and leading in local scientific data dissemination (leading and presenting at conferences, advisory boards, etc., and overseeing the development of the scientific content of educational programs). These responsibilities are generally related to latephase and marketed compounds, but can also include early phase trials (for example, phase I and II trials). The CRP is responsible for collaborating with the global teams in the planning, startup and conduct of phase 3b/4 studies (and phase I and II studies where applicable), as well as non clinical trial solutions/activities that are conducted in affiliates/countries as described in the clinical plan. In addition, the CRP, if assigned by the Director Medical and/or Regional Medical Leader, is responsible for support of global Development studies conducted in affiliates/countries. The core job responsibilities mayinclude those listed below as deemed appropriate by line management, as well as all other duties as assigned.