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. You will provide therapeutic, drug development expertise, 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.
Ideal candidates Must Have a Medical degree and ideally with Board Certification or country specialization in Ophthalmology. Board Certification is preferred but not a must. Experience in Clinical Research experience within Academia, Pharmaceutical, Biotech or other CRO industry. We are seeking candidates with the ability to review and evaluate clinical data and excellent oral and written communication skills.