Medical Director
Eureka Infotech Inc · Austin, TX
Apply & track with Apply EdgeThe role will oversee clinical development, medical monitoring, regulatory strategy, and medical affairs while working closely with KOLs, external experts, CROs, and cross-functional teams.Key ResponsibilitiesProvide medical oversight for clinical trials across multiple therapeutic areas.Support clinical development plans, protocols, medical monitoring, and data interpretation.Contribute to INDs, regulatory submissions, and health authority interactions.Build and manage KOL, consultant, and scientific advisor networks.Lead scientific advisory boards and external expert engagement.Develop medical affairs capabilities, publications, presentations, and educational materials.Collaborate with Clinical Operations, Regulatory, and other cross-functional teams.Represent the organization at scientific conferences and medical meetings.Required QualificationsMD or equivalent medical degree with an active medical license.Experience in pharmaceutical/biotech drug development, particularly early-stage programs.Experience with biologics development, clinical trials, and medical monitoring.Strong understanding of the drug development lifecycle from IND through commercialization.Experience working with FDA and international regulatory agencies.Strong scientific writing, communication, analytical, and organizational skills.Ability to work across multiple therapeutic areas in a fast-paced biotech environment.PreferredBoard certification in Internal Medicine, Oncology, Immunology, or a relevant specialty.Startup/emerging biotech experience.Experience managing programs across multiple therapeutic areas.Medical affairs or medical leadership experience.Experience working with CROs and external clinical development partners.