BlueRock is recruiting a key member of the Clinical Development group to support and direct preclinical, translational IND-enabling, and clinical development activities of the neurology programs. In this newly created role, the Medical Director Neurology will be charged with providing scientific and medical leadership and support for BlueRock’s neurology programs. Provide expert scientific and medical support and leadership to both preclinical and clinical stage BlueRock programs Support development and progression of a robust BlueRock neurology pipeline Medical monitoring and clinical review of active programs and studies Establish strong relationships with thought leaders in the field Represent the company in the neurology space both internally at meetings and externally, including global conferences Support the neurology pipeline by contributing to the assessment of potential new products or programs Work with cross-functional teams, and contribute to strong, collaborative efforts to strengthen internal capabilities Lead, contribute to, and provide oversight to development of clinical documents Contribute to the analysis, interpretation and reporting of preclinical and clinical data Provide clinical and scientific content and detailed review for regulatory documents, and contribute to the overall strategy in regulatory submissions and interactions Provide strategic programmatic input through interaction with the development leadership team Provide mentorship and support to more junior team members

• 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.

• Interpreting clinical data according to medical standards, GCP guidelines, study protocols, charter definitions, and Clario SOPs • Completing source documents accurately and promptly per protocol and SOP requirements • Correcting entries on source documents and Case Report Forms (CRFs) in a timely manner • Participating in protocol‑specific and ongoing training • Performing Photo Image Quality Assessment (Photo IQA) and participating in the medical photography process • Reviewing protocols, charters, and associated clinical and technical documents • Maintaining security and confidentiality of images, data, equipment, study materials, and subject information • Participating in sponsor site visits and audits as needed • Collaborating with management to address and resolve oncology‑related study concerns • Maintaining continuing professional medical education • Conducting quality control to ensure completeness and accuracy of assigned work • Identifying and supporting performance improvement initiatives • Contributing to the development, review, and evaluation of SOPs and study‑specific procedures • Creating oncology‑specific test cases for training • Maintaining a safe work environment and promptly reporting hazards • Participating in the Medical Affairs lecture series • Performing other duties as assigned by Medical Affairs leadership

Utilization Review Specialist: Responsible for ensuring adherence to Mindful Health’s utilization review plan by evaluating the efficiency, effectiveness, and medical necessity of outpatient services, including admissions and extended treatment. Establish processes to verify the medical necessity and appropriateness of outpatient admissions Conduct concurrent reviews to ensure extended stays are justified and properly documented Track patient lengths of stay and continued-stay days Refer non-compliant cases to the Physician Advisor for further evaluation Collaborate with the Utilization Review Committee to identify and resolve review-related issues Flag quality-of-care concerns and escalate them to the Quality Assurance Committee Coordinate with Social Services to support timely discharge planning Prepare and present monthly utilization reports and key metrics