Eyconis, Inc

• The Medical Director will serve as a key medical leader at Eyconis, providing strategic, scientific, and operational leadership across clinical development programs. • This individual will play a pivotal role in shaping and executing the company’s clinical strategy, ensuring scientific and medical rigor throughout all stages of development—from first-in-human studies through late-stage clinical trials. • The role reports directly to the Chief Medical Officer (CMO) and requires close collaboration with cross-functional teams, including Clinical Operations, Regulatory Affairs and CMC/Tech Operations. • Lead the design, implementation, and oversight of clinical development plans and protocols in ophthalmology. • Provide medical leadership across programs, ensuring alignment with Eyconis’ clinical and corporate strategy. • Author or review clinical documents, including protocols, investigator brochures, clinical study reports, and regulatory submissions (IND, NDA, BLA). • Contribute to the strategic planning of development milestones and portfolio prioritization. • Serve as the medical monitor for ongoing clinical trials, ensuring safety, integrity, and compliance with ICH/GCP standards. • Interpret clinical data and support data-driven decision-making across the development continuum. • Collaborate with internal and external stakeholders (CROs, investigators, KOLs) to ensure medical and operational excellence. • Support the CMO in shaping the clinical vision and long-term R&D roadmap. • Provide clinical insight and due diligence for potential partnerships or in-licensing opportunities. • Represent Eyconis at key scientific, medical, and regulatory meetings. • Contribute to scientific publications, abstracts, and presentations that advance the company’s thought leadership in ophthalmology. • Partner with Regulatory Affairs on strategy and communication with health authorities (FDA, EMA, PMDA). • Collaborate with nonclinical and translational research teams to bridge preclinical and clinical development. • Engage with Medical Affairs, Market Access, and Commercial colleagues to ensure alignment on clinical value propositions.

The Medical Director will serve as a key medical leader at Eyconis, providing strategic, scientific, and operational leadership across clinical development programs. This individual will play a pivotal role in shaping and executing the company’s clinical strategy, ensuring scientific and medical rigor throughout all stages of development—from first-in-human studies through late-stage clinical trials. The role reports directly to the Chief Medical Officer (CMO) and requires close collaboration with cross-functional teams, including Clinical Operations, Regulatory Affairs and CMC/Tech Operations. Key Responsibilities Clinical Development Leadership - Lead the design, implementation, and oversight of clinical development plans and protocols in ophthalmology. - Provide medical leadership across programs, ensuring alignment with Eyconis’ clinical and corporate strategy. - Author or review clinical documents, including protocols, investigator brochures, clinical study reports, and regulatory submissions (IND, NDA, BLA). - Contribute to the strategic planning of development milestones and portfolio prioritization. Medical Oversight and Execution - Serve as the medical monitor for ongoing clinical trials, ensuring safety, integrity, and compliance with ICH/GCP standards. - Interpret clinical data and support data-driven decision-making across the development continuum. - Collaborate with internal and external stakeholders (CROs, investigators, KOLs) to ensure medical and operational excellence. Scientific and Strategic Contributions - Support the CMO in shaping the clinical vision and long-term R&D roadmap. - Provide clinical insight and due diligence for potential partnerships or in-licensing opportunities. - Represent Eyconis at key scientific, medical, and regulatory meetings. - Contribute to scientific publications, abstracts, and presentations that advance the company’s thought leadership in ophthalmology. Cross-Functional Collaboration - Partner with Regulatory Affairs on strategy and communication with health authorities (FDA, EMA, PMDA). - Collaborate with nonclinical and translational research teams to bridge preclinical and clinical development. - Engage with Medical Affairs, Market Access, and Commercial colleagues to ensure alignment on clinical value propositions.