Clinical Research Coordinator – Phase – Miami, FL First-in-human, SAD​/MAD and dose-escalation studies

Ready to take your clinical research career deeper into Phase I?

Join a leading early-phase research site delivering first-in-human, SAD/MAD and dose-escalation studies
, working directly with Investigators, Sponsors and CROs.

You’ll play a hands-on role in participant screening, dosing, safety assessments, PK/PD sampling, study visits and clinical documentation – making a direct impact on bringing new therapies into development.

• Coordinate Phase I studies from start-up through close-out.
• Manage participant screening, enrolment, dosing and follow-up
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• Support SAD/MAD, dose-escalation and FIH studies
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• Coordinate vital signs, ECGs, labs, PK/PD sampling and safety assessments.
• Monitor and document AEs, SAEs and protocol deviations
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• Maintain accurate source documentation and EDC/eCRF data
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• Work closely with Investigators, Sponsors, CROs and clinical teams
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• Support monitoring visits, audits and inspections.

• 2+ years’ clinical research experience.
• Direct Phase I experience is essential.
• Experience in a Phase I unit, early-phase site or SMO
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• Strong understanding of ICH-GCP and FDA requirements
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• Experience with participant screening, dosing and safety assessments.
• Excellent organisation, attention to detail and communication skills.