Job Overview We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our dynamic research team. The ideal candidate will possess a strong foundation in clinical trials management, patient care, and regulatory compliance. As a Clinical Research Coordinator, you will be responsible for overseeing the daily operations of clinical studies, ensuring adherence to protocols, and maintaining accurate documentation. This role offers an exciting opportunity to contribute to innovative medical research that advances healthcare outcomes while working in a collaborative and fast-paced environment. Responsibilities Coordinate all aspects of clinical trials, including participant recruitment, screening, enrollment, and follow-up visits. Monitor patient safety and collect vital signs, blood samples, and other clinical data in accordance with study protocols. Review and verify study documentation for accuracy, completeness, and regulatory compliance. Manage data collection and entry using electronic medical record (EMR) systems and adhere to CDISC standards for data management. Ensure compliance with FDA regulations, ICH ,IRB, GCP guidelines, HIPAA privacy rules, and institutional policies throughout the research process. Supervise research staff and collaborate with multidisciplinary teams to facilitate smooth trial operations. Maintain thorough knowledge of clinical laboratory procedures, blood sampling techniques, and phlebotomy standards. Prepare reports on study progress, adverse events, and regulatory documentation for review by principal investigators and sponsors. Skills Proven supervising experience in clinical research settings with strong leadership capabilities. Extensive knowledge of clinical trials management, including protocol adherence and regulatory requirements. Proficiency in medical terminology, clinical laboratory procedures, and data management software such as statistical tools. Familiarity with EMR systems, FDA regulations, HIPAA compliance, and ICH GCP certification from a recognized issuer. Strong analysis skills with the ability to interpret clinical data accurately and efficiently. Experience in clinical development processes including patient monitoring, blood sampling, and vital signs assessment. Knowledge of CDISC standards for data collection and documentation review practices to ensure quality control. Join us in advancing medical science through meticulous research coordination that upholds the highest standards of integrity and excellence!

Qualifications:

Prior clinical research or healthcare experience preferred. (ophthalmology experience a plus, but not required) Strong organizational skills and attention to detail. Excellent communication and interpersonal skills. Ability to work independently and as part of a team. Why Join Us? Competitive compensation with growth potential Flexible scheduling Supportive and collaborative work environment Opportunity to be involved in cutting-edge retinal research

Pay:

$49,000.00 - $60,000.00 per year

Benefits:

Flexible schedule

Work Location:

In person