Qualifications include: MD (or DO, or an equivalent non-US medical degree) is required Minimum of 5 years of experience in clinical development in the biotechnology, pharmaceutical, or CRO setting, or equivalent academic clinical research experience, including hands-on experience as a medical monitor or in safety review of clinical trials Preferred: board certification or eligibility in Infectious Diseases, Gastroenterology/Hepatology, or Internal Medicine; direct experience in virology / infectious disease will be considered uniquely qualified Clinical trial experience either in the academic setting (as an investigator or sub-investigator) or in industry (as a director or medical monitor) with hands-on patient care and clinical practice experience Thorough understanding of GCP and familiarity with relevant FDA and ICH guidance, including adverse event management and safety reporting requirements Working knowledge of statistics as applied to clinical trial design and analysis Ability to think analytically and strategically to formulate, develop, and execute clinical plans Experienced with engaging internal and external expert physicians, scientists, and other key stakeholders in constructive scientific and clinical dialog around study design, study conduct, and interpretation of clinical results Experience working with CROs and other external resources, including oversight of CRO medical monitors Preferred: experience interacting with regulatory agencies (e.g., FDA, EMA) on clinical development programs Demonstrated ability to work in a team environment. Summary: This is an opportunity to work in a dynamic role, supporting the development of clinical study strategy and managing the subsequent protocol development, execution, interaction with regulatory agencies and ethics committees, medical monitoring, interpretation and presentation of clinical trials associated with the clinical development of novel and innovative drugs for viral diseases and other indications.