• Synthesize disparate facts from multiple sources and coalesce into an accurate and useful analytic product • Conduct thorough and comprehensive system-wide currency, business case and return on investment analysis for healthcare operations within the Military Health System (MHS), Veterans Administration (VA) or private sector • Execute data analytics processes to include data extraction, transformation, and loading; data visualization applications and techniques; and quantitative data analysis • Communicate in writing complex concepts and their effects/impacts on the target environment, such that a lay audience is capable of understanding • Identify and implement solutions to improve clinical and business data quality • SQL, R, and/or Python proficiency preferred • Tableau visualization experience preferred • Performs other job-related duties as assigned

• Support study execution across start-up, conduct, and close-out phases • Serve as a primary point of contact for assigned clinical sites and CRO field CRAs/monitors • Communicate directly with sites and CRO partners to obtain updates, resolve issues, and support study timelines • Support site initiation, ongoing site management, and site close-out activities • Assist with identification, documentation, tracking, and follow-up of site issues • Support oversight of CRO monitoring activities • Review monitoring visit reports and follow up on action items and unresolved findings • Track monitoring deliverables and escalate issues to the Associate Director, Clinical Operations as appropriate • Support inspection readiness and audit activities • Maintain accurate tracking tools for assigned studies, including: • Site start up and activation status • Subject enrollment and visit status • Essential document collection and TMF status • Vendor reconciliation • Assist with preparation of study status reports and metrics • Collect, review, and track site regulatory documents for completeness, accuracy, and compliance with applicable SOPs and regulatory requirements • Ensure timely filing of documents in the TMF/eTMF in accordance with TMF plans • Perform TMF quality control activities and support TMF audits and study close out • Support organization and coordination of internal team meetings, investigator meetings, and other study related meetings • Prepare meeting materials, take meeting minutes, and maintain action item logs • Support communication of study updates to internal stakeholders

• Analyze research requests and define the best approach to successfully complete them • Gather data, verify it for accuracy, and package it in a structured and easily digestible manner • Assess existing research sources and data collection strategies, while coming up with suggestions when possible • Collaborate with clients and managers on the status of your work • Use your creativity and expertise to support Infomineo’s internal development projects

Role Description 4DMT seeks a motivated and detail-oriented In-House Clinical Research Associate (IHCRA) to support the Company’s clinical trial activities. This position reports to the Associate Director, Clinical Operations, and will support the day-to-day execution of a Phase 3 clinical trial, including study start-up, conduct, and close-out activities. The IHCRA will serve as a key liaison between 4DMT, clinical sites, and CRO partners, with a focus on site support, monitoring oversight, regulatory compliance, and data quality. This role requires strong written and verbal communication skills, excellent organizational skills, and the ability to manage competing priorities while delivering high-quality work in a fast-paced, team-oriented environment. Qualifications - A. or B.S. degree required - Minimum of 1-2 years of experience supporting clinical trials in a sponsor or CRO environment - Experience supporting Phase 3 clinical trials preferred - Ophthalmology preferred - Working knowledge of clinical trial operations and ICH GCP guidelines - Experience with TMF/eTMF systems (Veeva Vault preferred) - Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) - Strong organizational skills and attention to detail - Ability to manage multiple priorities and meet deadlines - Strong interpersonal skills and ability to collaborate effectively with cross-functional teams and external partners - Willingness to travel as business needs demand (<5% anticipated) Requirements - Support study execution across start-up, conduct, and close-out phases - Serve as a primary point of contact for assigned clinical sites and CRO field CRAs/monitors - Communicate directly with sites and CRO partners to obtain updates, resolve issues, and support study timelines - Support site initiation, ongoing site management, and site close-out activities - Assist with identification, documentation, tracking, and follow-up of site issues - Support oversight of CRO monitoring activities - Review monitoring visit reports and follow up on action items and unresolved findings - Track monitoring deliverables and escalate issues to the Associate Director, Clinical Operations as appropriate - Support inspection readiness and audit activities - Maintain accurate tracking tools for assigned studies, including: - Site start up and activation status - Subject enrollment and visit status - Essential document collection and TMF status - Vendor reconciliation - Assist with preparation of study status reports and metrics - Collect, review, and track site regulatory documents for completeness, accuracy, and compliance with applicable SOPs and regulatory requirements - Ensure timely filing of documents in the TMF/eTMF in accordance with TMF plans - Perform TMF quality control activities and support TMF audits and study close out - Support organization and coordination of internal team meetings, investigator meetings, and other study related meetings - Prepare meeting materials, take meeting minutes, and maintain action item logs - Support communication of study updates to internal stakeholders - Support ad hoc Clinical Operations projects as assigned - Other duties as assigned Benefits - Compensation range: $38.00 TO 52.00 /HOURLY - Please note, the compensation range and actual rate offered to the final candidate depends on various factors: candidate’s geographical location, relevant work experience, skills, and years of experience. Company Description 4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company’s lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company’s lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company’s second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery.