Essential Skills: • Excellent written, verbal and interpersonal, relationship-building and negotiating communication skills • Excellent organizational skills to support project planning across multiple activities, anticipate and prioritize workload • Excellent teamwork skills. Organized; attention to detail and able to meet timelines in a fast-paced environment • Excellent analytical and problem solving skills, demonstrated ability to identify and understand complex issues and problems and identify and query key findings from study data and publications • Experience in public health or Internal Medicine (general or subspecialty) is highly desirable, in addition to clinical patient care. • Experience in developing effective abstracts, manuscripts, posters and slides and presenting at scientific meetings • Must be fully cognizant and adhere to regulatory and legal (Business Conduct) requirements for clinical trials and other Medical Affairs activities; thorough knowledge of FDA regulations, ICH guidelines and GCPs governing the conduct of clinical trials • Must be able to work with autonomy and independence • Ability to work around international time zones and ability to travel to and participate in domestic and international conferences which will include occasional weekend travel is required • Ability to work in a global environment which will require participation in meetings outside of standard work hours and on the weekends to accommodate time zone differences
Knowledge, Experience & Skills • Bachelor's degree a minimum, but M.D., D.O., PhD (biological or pharmaceutical sciences), or PharmD preferred. Prior experience in hepatology, infectious diseases, virology or clinical virology a plus. • Preferred experience in Medical Affairs and/or Clinical Research including Phase IIIb and IV studies; clinical trials management, medical monitoring and scientific expertise