Medical Director – Hemato-Oncology
Location – Poland or any EU
This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. You will provide medical support to ICON project teams on clinical issues to ensure that clinical studies are conducted according to the highest ethical principles and in compliance with applicable legal and regulatory standards. This position will report to the VP Medical Affairs or designee.
Overview of the RoleProvide therapeutic and drug development expertise, oversee drug safety associates providing adverse event reporting, follow up on adverse events as necessary and interact with Sponsors and investigative sites on protocol medical issues.Contribute to investigator meeting presentations, review study documentation, oversee safety data review and provide medical support to Business Development.Senior level candidates will be expected to have prior management experience and serve as product development consultants to Clients.
Role Requirements / Skills / Experience Required Medical degreeBoard certification in Hematology, oncology or bothMinimum 2 years’ experience that includes academic experience coupled with Pharmaceutical, Biotech or CRO experience.Ability and willingness to travel on an as needed basis.Ability to review and evaluate clinical data.Excellent oral and written communication skills.