Travel CRC
On-site · Lake Mary, Florida, United States
Job Summary
Clinical Research Coordinator position at Alcanza supporting multi-site Phase I-IV studies across multiple therapeutic areas. Responsible for screening patients for enrollment, obtaining consents, scheduling visits, performing source documentation, entering data in EDC, recording vital signs and ECGs, coordinating lab procedures and specimen handling, managing medical record requests, logs, supplies, and study documents; conducting monitoring visits, reporting adverse events and deviations, ensuring regulatory compliance (GCP, ICH, HIPAA, FDA, SOPs), assisting with recruitment, and coordinating site initiation and Investigator Meetings. Requires Medical Assistant diploma, LPN/LVN, EMT credential or an Associate’s degree with at least 1 year of clinical research/clinical experience; bilingual English/Spanish is a plus; strong communication, organizational, and confidentiality skills; able to work with investigators, staff, subjects, and external partners. Benefits include health, dental, vision, life, disability, HSA, and 401k with match. Location: Lake Mary, Florida (onsite).
Required Qualifications
- A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate’s degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience
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