(Senior) CRA - Miami

This is an exciting opportunity for an experienced Clinical Research Associate or Senior Clinical Research Associate to support the clinical development efforts of a respected international organisation. With a strong commitment to improving patient outcomes through high-quality research, they lead studies across diverse therapeutic areas, operating under rigorous standards that place patient safety and scientific integrity at the forefront. Contractors here play a crucial role in progressing meaningful studies, working with innovative methodologies that include on-site, remote and risk-based monitoring.

Your role as Clinical Research Associate / Senior Clinical Research Associate

• Oversee investigational sites from start-up to close-out, delivering on-site, remote or hybrid monitoring in line with study timelines and protocols.

• Maintain clear, proactive communication with sites, project teams, and sponsors to keep studies running smoothly.

• Support study start-up activities, including site identification, feasibility assessments and selection.

• Deliver protocol training to site staff and ensure investigational products are correctly managed, stored and documented.

• Perform thorough source document review and verification, and collaborate on query resolution within EDC systems.

• Manage essential documents and ensure the completeness and accuracy of the site-level Trial Master File.

Experience and qualifications for the Clinical Research Associate / Senior Clinical Research Associate role

• University degree or equivalent experience, ideally with a background in health sciences; advanced degrees welcome but not essential.

• Minimum of 3 years' experience as a CRA within pharmaceuticals, biotech or CRO environments.

• Strong grasp of GCP principles with proven ability to apply them in day-to-day monitoring.

• Familiarity with clinical study phases, local regulatory approval processes, and standard clinical systems (EDC, CTMS, eTMF, IXRS).

• Excellent communication skills, detail-focused, and adept at problem-solving to keep studies compliant and on track.

• Comfortable with extensive travel and overnight stays, holding a valid passport with at least six months remaining.

For immediate consideration, or to learn more about similar contract opportunities in clinical research, apply today or reach out directly.