A market leading CRO
The successful candidate will provide medical and scientific advisory expertise and will serve as regional and/or global Medical Advisor on assigned projects..
They will be engaged on a variety of clinical trials in the preparation and project delivery lifecycle. They will serve as Scientific Advisor and provide guidance to Project Leaders on the medical and scientific aspects of assigned projects.
Providing medical support to investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility. They will also perform medical review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs).
The Successful Applicant
The successful candidate will have a Medical degree from an accredited and internationally recognized medical school.
They will have particular expertise in Infectious Diseases
The ideal candidate will have experience in clinical trials either as investigator, co-investigator, or from working either for a pharmaceutical business or CRO, ideally as a medical monitor.
They will also have an excellent command of written and spoken English, and will have strong communication, presentation and interpersonal skills.
What's on Offer
A fantastic career with a market leading CRO.
The opportunity to work on a variety of leading clinical trials.
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