Clinical Research Coordinator I
$55,000–$65,000 year
On-sitePhoenix, Arizona, United States
Job Summary
Execute study-related activities from startup through closeout in compliance with GCP, ALCOA-C principles, and sponsor requirements. Coordinate patient visits including demography, vitals, EKG, phlebotomy, drug administration, and physical exams while assisting the Principal Investigator with informed consent and direct patient care procedures. Maintain source documents, investigational drug accountability, and regulatory records; enter source data into EDC and resolve queries. Communicate with contract research organizations, IRB, sponsors, and vendors to manage trial needs. Process prescriptions, prior authorizations, and patient education enrollments. Scan correspondence into EMR and prepare documentation for sponsor meetings. Perform blood and urine sample processing per IATA and OSHA standards.
Required Qualifications
- At least 1 year of research experience
- At least 1 year of direct patient experience
- Meticulous detail orientation
- Professional attitude
- Reliability
- Organizational skills to support accurate record-keeping
- Ability to follow verbal and written instructions
- Interpersonal skills to work as a team with patients and outside parties
- Effective communication in English, both verbally and in writing, with proper grammar and spelling skills
- Mathematical and analytical ability for basic to intermediate problem solving
- Basic to intermediate computer operation
- Proficiency with Microsoft Excel, Word, and Outlook
- Specialty knowledge of systems relating to job function
- Knowledge of state and federal regulations such as ICH GCP, IATA
- General understanding of HIPAA guidelines
Desired Qualifications
- Working knowledge of all applicable protocols
- Experience as the primary coordinator for a specific protocol
- In-depth knowledge of a specific protocol
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