Role OverviewThe ideal candidate will have a strong background in clinical research, excellent organizational skills, and the ability to coordinate research activities while ensuring compliance with study protocols and regulatory requirements.
What You Will Do
Coordinate and manage day-to-day activities for assigned clinical research studies, ensure study activities are conducted according to protocols, regulatory requirements, and company policies.
Why It Might Be a Fit
The candidate should have experience working in a clinical research, healthcare, or academic research setting, familiarity with electronic data capture (EDC) systems and clinical research databases, and knowledge of Good Clinical Practice (GCP) guidelines.
Requirements
- Bachelor’s degree in a health-science-related field
- Minimum of 2 years of experience working as a Clinical Research Coordinator
- Experience coordinating clinical research studies from start-up through completion
- Strong understanding of clinical research protocols, regulatory requirements, and documentation
- Excellent organizational, communication, and interpersonal skills
- Ability to manage multiple priorities and meet study deadlines
- Strong attention to detail and commitment to maintaining accurate research records
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