Clinical Service company has an immediate opportunity for an Associate Director, Director OR Senior Director (Oncology) in Medical Affairs (title determined commensurate with experience - can be based out of any company office).
You will provide medical support to 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. The Associate Director, Director OR Senior Director will report to the VP Medical Affairs or designee.
Responsibilities include, but are not limited to:
Provide 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 CRF safety 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.
Medical degree with board certification in Oncology.
Minimum 2-5 years experience that includes both academic and pharma, biotech or CRO.
Ability and willingness to travel on an as needed basis.
Ability to review and evaluate clinical data.
Excellent oral and written communication skills.