Clinical Research Coordinator I
On-site · Maplewood, Minnesota, United States
Job Summary
Clinical Research Coordinator I at Headlands Research (Maplewood, MN) coordinates all aspects of assigned clinical trials from site initiation to close-out, conducts subject visits, ensures compliant documentation per ALCOA-C, manages recruitment and informed consent, maintains data entry and query resolution, supports monitoring visits and inspections, and collaborates with investigators, sponsors/CROs, and internal teams. Requirements include a Bachelorâs degree or equivalent healthcare-related education/experience, prior CRC experience, familiarity with EDC/IVRS, strong knowledge of FDA/ICH-GCP regulations, and excellent communication and organizational skills. This onsite role operates MondayâFriday 8:00amâ4:30pm with full-time benefits and a mission-driven culture.
Required Qualifications
- Bachelor's degree OR 2 years of college in a health-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP
- Previous experience as a Clinical Research Coordinator
- Industry-sponsored trial experience strongly preferred
- Familiarity with electronic data capture (EDC), IVRS, and other trial platforms
- Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures
- Proficiency in medical terminology and clinical documentation practices
- Strong interpersonal, verbal, and written communication skills
- Organized, detail-oriented, and capable of managing multiple priorities
- Proficient in Microsoft Office and other clinical research systems
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