Senior Clinical Research Associate - Cra

Job Description 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.Compensation:$65 - $90 hourlyResponsibilities:Coordinate with study teams to support the successful initiation and execution of clinical trialsIdentify, evaluate, and qualify investigators and research sites within the Dallas region and surrounding areasPrepare and review essential documentation required for site initiation and regulatory readinessConduct on-site monitoring visits and remote monitoring activities while maintaining detailed documentation of findings and follow-up actionsCollaborate with Clinical Trial Managers and Project Managers to escalate site concerns and resolve operational challengesReview study data on an ongoing basis to identify discrepancies, missing information, or protocol deviationsSupport the full monitoring lifecycle, including pre-study visits, site initiation visits, routine monitoring visits, and close-out visitsVerify that informed consent procedures and protocol requirements are properly followed to protect research participantsTrack and follow up on adverse events and serious adverse events while ensuring appropriate reporting procedures are followedEnsure the accuracy and integrity of case report form data through a comprehensive source document reviewMaintain compliance with study monitoring plans, standard operating procedures, and regulatory guidelinesParticipate in investigator meetings, project team meetings, and study-related teleconferencesMaintain ongoing training related to ICH GCP, study protocols, and internal proceduresSupport regulatory documentation tracking, site performance evaluation, and study timeline adherenceQualifications:Five or more years of clinical research monitoring experience as a Clinical Research AssociateAt least three years of experience supporting studies in central nervous system indications, such as neurology or psychiatry-related therapeutic areasMinimum four years of experience working in contract-based CRA positions, such as independent contractor, consultant, or similar arrangementsExperience conducting site monitoring visits and managing investigator site relationshipsBachelor's degree from a four-year university, preferably in a scientific or health-related fieldCandidates with significant clinical research experience, nursing background, or relevant medical certifications may be considered in place of a traditional degreeAbility to work as an independent vendor through an established corporation or LLC with appropriate business insuranceMust have authorization to work in the United StatesMust be located within the greater Dallas areaAvailability to support studies for at least one yearStrong communication skills in English and the ability to navigate complex clinical research discussions using medical terminologyProfessional communication skills with the ability to collaborate effectively across study teams and research sitesClinical research certifications, such as CCRA, CCRP, or similar credentials, are beneficial but not requiredAbout CompanyC-Clinical – Dallas Area OpportunitiesC-Clinical in Dallas supports clinical operations across the pharmaceutical, biotechnology, and medical device industries, with opportunities throughout Dallas and the surrounding region.Our foundation is built on meaningful relationships and a commitment to service—guided by the principle of "love your neighbor as yourself." We approach our work with the care and intention we'd give to family, not out of obligation, but out of purpose.C-Clinical exists because we believe in the power of life-changing medical research and the impact it can have on communities. We've built this company to do what we love—contribute our time, talents, and resources to those who need them most.If you're in the Dallas area and passionate about advancing medical research with integrity and purpose, we invite you to connect with us.