Clinical Research Coordinator 1
On-site · Mobile, Alabama, United States
Job Summary
Coordinate clinical trials per FDA requirements and GCP guidelines per sponsor protocols; manage adverse event reporting, informed consent, and protocol deviations; ensure ALCOA-compliant documentation; phlebotomy and specimen handling; communicate with sponsors, CROs, IRBs, laboratories, and clinical personnel; travel to investigator meetings; provide study education to subjects and oversee diary completion; promote team mentality and flexible hours as needed; maintain familiarity with ongoing studies and assist with monitors during onsite visits.
Required Qualifications
- 1 year of experience in clinical research
- Completion of formal medical training, educational program, or healthcare experience
- Strong medical terminology
- Ability to perform clinical, laboratory, and diagnostic tests (vital signs, height, weight, etc.)
- Ability to work independently and lead study-related tasks
- Ability to multi-task in a high-paced evolving environment
- Excellent organizational and task management skills
- Fluent in English
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