Clinical Research Coordinator - 254932

• *Seeking a Clinical Research Coordinator in San Marcos, TX**

Job Description

Are you passionate about clinical research and improving patients’ lives? Are you looking to grow your clinical skills and ophthalmic knowledge in a stimulating and supportive setting? If so, we invite you to consider this exciting role.

Key Responsibilities

• Coordinate ophthalmic clinical trials (Phases I–IV) with a focus in retina.
• Serve as a lead coordinator across multiple studies, working as both masked and unmasked CRC.
• Manage EDC data entry, complete system-specific trainings, and resolve data queries.
• Recruit, screen, and retain study participants, including medical history documentation and review.
• Perform subject assessments including vitals, lab draws, and diagnostic testing.
• Maintain and organize regulatory documents in compliance with sponsor and CRO requirements.
• Collaborate with study sponsors, monitors, and CROs throughout the clinical trial lifecycle.
• Oversee investigational product (IP) management, including training, storage, temperature monitoring, shipping/receiving, dispensing/destruction, and accountability logs.
• Conduct IP inventory, reconciliation, and ensure protocol compliance for administration.
• Support site feasibility assessments, qualification visits, and study questionnaires.
• Partner with CRO teams on study submissions, continuing reviews, adverse event reporting, query resolution, and study close-out.

Location: San Marcos, TX

Pay rate: $65-85K (Depending on experience)

Schedule: Full time, onsite, 40 hrs a week