Part time Pharmacovigilance Physician

We are seeking a Drug Safety Physician to work 2-3 days a week who will be responsible for assessment and reporting of adverse events, with responsibility for post marketed safety reports, writing PSURs, and act as deputy QP. The team have primary responsibility for the medical evaluation of define global adverse event reports, including all serious and expedited reports, this role provides guidance and direct participation in the follow-up determination for adverse events, as medically required. They will also participate in review of selected aggregate reports in conjunction with surveillance function of the pharmacovigilance organisation with respect to accuracy, content and signal detection.

You will be a fully GMC registered physician with broad clinical and drug safety knowledge in post marketing and clinical safety. You will also have demonstrated ability to work in a matrix organisation with a sound knowledge of general medicine and clinical practice. A familiarity with industry principles of drug development, pharmacology, bio statistics, clinical trial methodology and pharmacoepidemiology is preferred.

For full details please call Anna 020 922 7141

This position, Part time Pharmacovigilance Physician, was posted on February 8, 2010. Since this job has been published, it has been viewed 34 times.