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Clinical Research Coordinator

Northshore Research Associates LLC • Olla, LA, US • published 2026-10-11 21:03:18.432945

Description

**Job Summary** The Clinical Research Coordinator will manage the day\-to\-day conduct of clinical trials, including participant screening, enrollment, and follow\-up according to study protocols. Daily tasks include obtaining and documenting informed consent, scheduling and conducting study visits, collecting and entering source data, and maintaining accurate study records. The coordinator will collaborate with investigators, sponsors, and regulatory staff to ensure protocol compliance, support monitoring visits, and assist with regulatory submissions and reporting. The role also involves educating participants about study procedures, safeguarding participant safety, and helping optimize study workflows to meet timelines and quality standards. **Qualifications** * Demonstrated clinical research experience, including involvement in clinical trials and familiarity with Good Clinical Practice (GCP). * **Ability to manage informed consent processes, ensuring clear communication, documentation, and participant understanding.** * Knowledge of study protocol requirements and the ability to implement and monitor protocol adherence in daily research activities. * **Strong research and data...

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