Clinical Trial Coordinator
4 days ago
**Job Summary**
**Duties**
- Planning, execution, and monitoring of clinical trials from initiation to completion.
- Analyze data collected during trials to ensure accuracy and integrity.
- File study related documents in Investigator Site Files (ISFs)
- Collaborate with cross-functional teams to facilitate effective communication and project progress.
- Conducting patient visits, performing informed consent process, filing Case Report Forms, collection of vital signs and biological samples, if required.
- Maintain comprehensive documentation related to trial activities, including patient records and study reports.
- Ensure compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements.
**Qualifications**
- Bachelor’s degree in Nursing, Life Sciences, or a related field; advanced degree preferred.
- Proven experience in clinical trial management or related roles within the healthcare or research sector.
- Strong knowledge of medical terminology and clinical research methodologies.
- Proficiency in data management systems and tools for effective data collection and analysis. (e.g. iMedidata, RedCap, EMR etc.)
- Strong analytical skills with attention to detail for accurate data interpretation.
- Ability to work collaboratively in a fast-paced environment while managing multiple priorities.
Pay: $45,000.00-$55,000.00 per year
**Benefits**:
- Dental care
- Extended health care
- Paid time off
Work Location: In person
Expected start date: 2025-08-15
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