Clinical Research Coordinator
United Consulting Hub
Seeking a Clinical Research Coordinator to support clinical trials, patient enrollment, study documentation, and regulatory compliance while ensuring adherence to GCP guidelines. Key Responsibilities Coordinate clinical study activities Maintain Trial Master File (TMF) documentation Schedule patient visits and study procedures Assist with informed consent documentation Support regulatory submissions and audit readiness Collaborate with investigators and study sponsors Qualifications Bachelor's degree in Life Sciences, Biology, Pharmacy, Nursing, or related field Basic knowledge of GCP and FDA regulations Strong communication and documentation skills #J-18808-Ljbffr United Consulting Hub
Vacancy posted 3 days ago
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