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Clinical Research Associate

2 months ago

Chattanooga, Tennessee, United States Wake Research Full time
Job Summary

We are seeking a highly skilled Clinical Research Coordinator to join our team at Wake Research. The successful candidate will be responsible for managing, supporting, and coordinating daily clinical trial activities, ensuring compliance with established research protocols and regulatory requirements.

Key Responsibilities
  • Study Coordination: Assist the trial Investigator in screening and reviewing potential study participants' eligibility, maintaining case report forms, charts, and documentation.
  • Data Management: Collect and enter data as necessary, ensuring accuracy and completeness.
  • Team Leadership: Mentor, train, and oversee other clinical research coordinators and research assistants, providing high-level guidance and support.
  • Regulatory Compliance: Ensure all clinical activities are carried out in accordance with established research protocols and regulatory requirements, including HIPAA guidelines.
  • Study Start-up and Close-out: Assist with study start-up, maintenance, and close-out, as needed, for those on the team.
Requirements
  • Experience: 1-2 years of experience as a Clinical Research Coordinator is ideal, but not required.
  • Education: Previous experience as a medical assistant, LPN, or RN is highly valued.
  • Skills: Excellent verbal and written communication skills, ability to learn quickly, read and understand complex protocols, and multi-tasking.
  • Certifications: Successful completion of GCP Certification and Advanced CRC is preferred.
What We Offer
  • Competitive Compensation: A competitive salary and benefits package, including 401(k) matching, dental insurance, disability insurance, and more.
  • Opportunities for Growth: A dynamic and innovative work environment where every team member contributes to global health advancements.