Job Description
Job Description
Senior CRA – Miami Area
C-Clinical is hiring a Senior Clinical Research Associate (CRA) with experience in CNS, oncology, or metabolic indications to join our growing team in the Miami area. This is a hybrid role that combines remote, risk-based monitoring with on-site visits as needed.
We’re seeking experienced professionals who are passionate about advancing clinical research and ready to make a meaningful impact. The ideal candidate is proactive, detail-oriented, and brings a strong understanding of regulatory requirements, site engagement, and protocol compliance.
At C-Clinical, we’re committed to life-changing work—and we want to grow with individuals who share that same drive. Our team values collaboration, integrity, and purpose in every study we support.
If you're a skilled CRA based in or around Miami and ready to contribute to a mission-driven research team, we’d love to connect.
Apply today and please complete the brief intro survey sent via email after submission.
Compensation:
$65 - $95 hourly
Responsibilities:
Sr. CRA – Miami Area (On-site/Hybrid)
- Interfaces with the study team to ensure timely initiation and completion of clinical trials
- Responsible for the identification, evaluation, and qualification of investigators and sites in the Miami area and surrounding region
- May prepare and submit essential document packages required for clinical site initiation
- Performs on-site monitoring activities for clinical trials and escalates site issues to the Clinical Trial Manager (CTM)/Project Manager (PM); documents activities in the monitoring reports and follow-up correspondence
- Reviews and manages data on-site and remotely; resolves issues on a continuous basis to achieve timely database targets
- May be responsible for all aspects of study site monitoring: pre-study visits, site initiation visits, routine monitoring visits, close-out visits of clinical sites, and maintenance of study files, with or without guidance
- Ensures the protection of research subjects by verifying that informed consent procedures and protocol requirements are followed in accordance with applicable regulatory requirements
- Identifies, tracks, and follows up on all Adverse Events (AEs) and Serious Adverse Events (SAEs); ensures all applicable SAEs are reported to appropriate regulatory authorities
- Ensures the accuracy and integrity of data submitted on electronic or paper case report forms (CRFs), or other data collection tools, through comprehensive source document review; monitors study databases for missing or discrepant data compared to source records
- Ensures that all monitoring tasks are performed according to site SOPs, established guidelines, work instructions, and project-specific plans (e.g., monitoring plan)
- Maintains study blinding and serves as a blinded study monitor as needed; conducts eCRF/CRF review, query generation, and resolution in line with established data review guidelines
- Attends investigator meetings, project team meetings, and teleconferences as required
- Understands and applies knowledge of local, state, and federal regulations (e.g., FDA, ICH-GCP)
- Maintains current training on ICH-GCP, study protocols, and internal procedures
- May track regulatory documentation, monitor recruitment progress, evaluate site quality and compliance, and help motivate assigned sites to meet deadlines and performance expectations
Qualifications:
- 3 years or more as a CRA with site monitoring responsibility And 1 year or more CNS
Or
- 3 years or more as a CRA with site monitoring responsibility And 1 year or more in either: Phase 1, a complex indication with in-patient monitoring, Or metabolic studies
Or
- 3 years or more as a CRA with site monitoring responsibility And 1 year or more in Oncology Monitoring
And
- The candidate possesses a 4-year university degree, ideally in a scientific field
- In lieu of a 4-year university degree, a candidate with 7 or more years of relevant clinical research experience, nursing/possibly another medical certification, and 5 years of monitoring in a complex indication (in-patient, oncology, phase 1, etc.) may be considered
- Must have working rights in the United States
- Must be located within the greater Miami area
- The candidate must have availability for at least 1 year
- Must possess exemplary verbal skills in the English language with the ability to solve complex problems using medical terminology
- Bi-lingual is a plus
- Corp to Corp
- Must be proficient at tactfully managing intra-team communication, as well as interpersonal communication
- Note: the travel rate is 50% regular rate
About Company
C-Clinical – Miami Area Opportunities
C-Clinical in Miami advances clinical operations throughout the pharmaceutical, biotechnology, and medical device industries, offering opportunities across Miami and the surrounding region.
At our core, we’re guided by service and compassion—rooted in the principle of “love your neighbor as yourself.” We treat each partnership with the same care and respect we would offer to family, leading not by obligation, but by purpose.
C-Clinical was founded to pursue what we’re passionate about: life-changing medical research. Our mission is to apply our time, talents, and expertise to help those who need them most—because real care makes real impact.
If you’re in the Miami area and believe in bringing integrity and heart to clinical research, we’d love to connect.