Cardiology Clinical Research Associate

Piper Companies; United States; Remote; USD 100,000 - 130,000; Full time

Benefits offered by this job

Comprehensive benefits

Job summary

Piper Companies is seeking a Cardiology Clinical Research Associate to support a growing cardiovascular clinical program with monitoring sites across the United States. You will perform site visits, review CRFs, ensure data integrity, and maintain regulatory compliance per ICH-GCP and FDA guidelines. Travel is required.

Competitive salary and comprehensive benefits. Join a dynamic team advancing cardiovascular trials in a fast-paced regulatory environment and contribute to high-quality data for

Qualifications

• Bachelor's degree in Life Sciences, Nursing or 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.

Responsibilities

• Monitor cardiology trials at sites to ensure protocol, GCP and regulatory compliance.
• Conduct site initiation, routine monitoring and close-out visits.
• Review source documents and CRFs for accuracy and completeness.
• Identify, document and resolve discrepancies in data.
• Collaborate with investigators, study coordinators and sponsors to ensure study success.
• Maintain thorough documentation of site activities and monitoring reports.
• Ensure adverse events and safety data are reported appropriately.

Skills

GCP knowledge

FDA regulations

EDC systems

CTMS tools

Travel readiness

Education

Bachelor's degree in Life Sciences

Tools

EDC systems

CTMS

Job description

Piper Companies is seeking a Cardiology Clinical Research Associate to support a growing clinical research program within the cardiovascular and medical device/pharmaceutical industry. The Cardiology Clinical Research Associate will be responsible for monitoring clinical trials, ensuring data integrity, and supporting investigative sites in compliance with regulatory standards and study protocols.

Responsibilities of the 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.
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• 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.

Requirements of the Cardiology Clinical Research Associate:

• 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.

Compensation for the Cardiology Clinical Research Associate:

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

Keywords: cardiology clinical research associate, CRA, clinical trials, cardiology studies, GCP, FDA regulations, monitoring visits, site management, EDC systems, data integrity, clinical research, pharmaceutical, medical device, cardiovascular trials

This job opens for applications on 9/17/2026. Applications for this job will be accepted for at least 30 days from the posting date.

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