PRINCIPAL MEDICAL WRITER jobs in USA, United Kingdom

At Houston Methodist, the Senior Scientific Writer is responsible for functioning as the mentor for junior staff... with an extensive knowledge of both medical and technical science while working with scientific and clinical teams to concisely...

Overview As a Principal Medical Writer you will be joining the world’s largest & most comprehensive clinical research... for review, and incorporate/resolve comments with all reviewers. Acts as a lead medical writer on complex programs and numerous...

or follow MMS on . Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze..., and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges...

or follow MMS on . Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze..., and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges...

or follow MMS on . Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze..., and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges...

or follow MMS on . Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze..., and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges...

or follow MMS on . Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze..., and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges...

or follow MMS on . Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze..., and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges...

or follow MMS on . Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze..., and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges...

or follow MMS on . Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze..., and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges...

or follow MMS on . Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze..., and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges...

or follow MMS on . Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze..., and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges...

or follow MMS on . Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze..., and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges...

or follow MMS on . Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze..., and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges...

or follow MMS on . Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze..., and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges...

or follow MMS on . Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze..., and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges...

or follow MMS on . Responsibilities Under minimal supervision, the Medical Writer will critically evaluate, analyze..., and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges...