JOB SUMMARY

We are seeking a dedicated and detail-oriented Clinical Trial coordinator to who executes clinical research studies from start-up phase to close-out. The ideal candidate will possess a strong background in clinical research, data management, and medical terminology. This role requires excellent analytical skills and the ability to multi-task effectively while ensuring compliance with regulatory standards.

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.
  If you are passionate about advancing medical research and have the skills necessary for this role, we encourage you to apply for the Clinical Trial Coordinator position.
  Job Type: Full-time
  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: 2025-08-1

• 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.