• Job Description

  Req#: 576862
  Description
  
  C-Clinical is looking for an experienced Senior Clinical Research Associate to support clinical trials across the Miami region. This opportunity is well-suited for professionals who enjoy working closely with investigative sites while ensuring strong oversight of complex clinical studies. The position includes both remote monitoring and on-site visits, offering a balanced approach that keeps you connected to study teams while maintaining flexibility in your work environment.
  
  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 Miami 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 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 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 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

• About the company

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