Cardiology Clinical Research Associate

• Monitor cardiology clinical trials at investigative sites to ensure adherence to protocols, GCP guidelines, and regulatory requirements.
• Conduct site initiation, routine monitoring, and close-out visits.
• Review source documents and case report forms (CRFs) for accuracy, completeness, and consistency.
• Identify, document, and resolve discrepancies in clinical data.
• Collaborate with investigators, study coordinators, and sponsors to ensure successful study execution.
• Maintain detailed documentation of site activities and monitoring reports.
• Ensure all adverse events and safety data are reported appropriately.

• Bachelor’s degree in Life Sciences, Nursing, or a related field.
• 2+ years of clinical research monitoring experience, preferably in cardiology trials.
• Strong knowledge of ICH-GCP guidelines and FDA regulations.
• Experience with EDC systems and clinical trial management tools.
• Excellent organizational, communication, and problem-solving skills.
• Ability to travel as required for site visits.

• $100,000 - $130,000 base salary
• Full Comprehensive Benefits:
  Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law.

This job opens for applications on 10/2/2026. Applications for this job will be accepted for at least 30 days from the posting date.

#LI-AG1

#REMOTE