C-Clinical is looking for an experienced Senior Clinical Research Associate to support clinical trials across the Dallas region. This opportunity is ideal for professionals who enjoy working closely with investigative sites while maintaining strong oversight of complex clinical studies. The position includes both remote monitoring and on-site visits, creating a balanced environment that allows you to stay engaged with study teams while maintaining flexibility. We are looking for individuals with a strong background in clinical monitoring and meaningful experience within central nervous system indications, such as neurology or psychiatry-related research. This position requires professionals who understand regulatory expectations, communicate effectively with site teams, and maintain a high level of attention to protocol compliance and data integrity. C-Clinical is committed to advancing meaningful research that improves patient outcomes. Our team values collaboration, professionalism, and scientific integrity, and we welcome individuals who take pride in contributing to well-run clinical trials. If you are a Senior CRA based in the greater Dallas area with strong CNS monitoring experience and are interested in working within a collaborative clinical research environment, we encourage you to apply. Responsibilities: • Coordinate with study teams to support the successful initiation and execution of clinical trials • Identify, evaluate, and qualify investigators and research sites within the Dallas region and surrounding areas • Prepare and review essential documentation required for site initiation and regulatory readiness • Conduct on-site monitoring visits and remote monitoring activities while maintaining detailed documentation of findings and follow-up actions • Collaborate with Clinical Trial Managers and Project Managers to escalate site concerns and resolve operational challenges • Review study data on an ongoing basis to identify discrepancies, missing information, or protocol deviations • Support the full monitoring lifecycle, including pre-study visits, site initiation visits, routine monitoring visits, and close-out visits • Verify that informed consent procedures and protocol requirements are properly followed to protect research participants • Track and follow up on adverse events and serious adverse events while ensuring appropriate reporting procedures are followed • Ensure the accuracy and integrity of case report form data through a comprehensive source document review • Maintain compliance with study monitoring plans, standard operating procedures, and regulatory guidelines • Participate in investigator meetings, project team meetings, and study-related teleconferences • Maintain ongoing training related to ICH GCP, study protocols, and internal procedures • Support regulatory documentation tracking, site performance evaluation, and study timeline adherence Qualifications: • Five or more years of clinical research monitoring experience as a Clinical Research Associate • At least three years of experience supporting studies in central nervous system indications, such as neurology or psychiatry-related therapeutic areas • Minimum four years of experience working in contract-based CRA positions, such as independent contractor, consultant, or similar arrangements • Experience conducting site monitoring visits and managing investigator site relationships • Bachelor’s degree from a four-year university, preferably in a scientific or health-related field • Candidates with significant clinical research experience, nursing background, or relevant medical certifications may be considered in place of a traditional degree • Ability to work as an independent vendor through an established corporation or LLC with appropriate business insurance • Must have authorization to work in the United States • Must be located within the greater Dallas area • Availability to support studies for at least one year • Strong communication skills in English and the ability to navigate complex clinical research discussions using medical terminology • Professional communication skills with the ability to collaborate effectively across study teams and research sites • Clinical research certifications, such as CCRA, CCRP, or similar credentials, are beneficial but not required Compensation: $65 - $90 hourly

• Coordinate with study teams to support the successful initiation and execution of clinical trials • Identify, evaluate, and qualify investigators and research sites within the Dallas region and surrounding areas • Prepare and review essential documentation required for site initiation and regulatory readiness • Conduct on-site monitoring visits and remote monitoring activities while maintaining detailed documentation of findings and follow-up actions • Collaborate with Clinical Trial Managers and Project Managers to escalate site concerns and resolve operational challenges • Review study data on an ongoing basis to identify discrepancies, missing information, or protocol deviations • Support the full monitoring lifecycle, including pre-study visits, site initiation visits, routine monitoring visits, and close-out visits • Verify that informed consent procedures and protocol requirements are properly followed to protect research participants • Track and follow up on adverse events and serious adverse events while ensuring appropriate reporting procedures are followed • Ensure the accuracy and integrity of case report form data through a comprehensive source document review • Maintain compliance with study monitoring plans, standard operating procedures, and regulatory guidelines • Participate in investigator meetings, project team meetings, and study-related teleconferences • Maintain ongoing training related to ICH GCP, study protocols, and internal procedures • Support regulatory documentation tracking, site performance evaluation, and study timeline adherence