Senior Clinical Research Associate - Cra

C-Clinical is seeking a Senior Clinical Research Associate to support clinical trials throughout the Miami region. The position combines remote responsibilities with routine on‑site monitoring visits, allowing flexibility and direct engagement with investigative teams. The ideal candidate has a strong background in clinical monitoring and hands‑on experience supporting central nervous system studies, including neurology and psychiatry indications. This role involves ongoing communication with investigators, coordinators, and sponsors while supporting data quality, patient safety, and study timelines across multiple research sites. 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 Miami 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 elevate 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 or 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 Miami 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 #J-18808-Ljbffr