Clinical Research Associate (Cardio - 174582

Piper Companies; United States; Remote; USD 100,000 - 135,000; Full time

Job summary

Piper Companies is seeking a Clinical Research Associate with a focus on cardiology or neurology to support trials in the pharmaceutical and biotech sectors. The role requires meticulous monitoring of studies, ensuring GCP compliance, and managing data across the trial lifecycle.

The CRA will conduct on-site and remote visits, review CRFs/eCRFs, and collaborate with investigators to ensure safe and compliant study execution while maintaining TMF documentation and monitoring reports.

Qualifications

• Bachelor's degree in Life Sciences, Nursing, or a related field.
• 2+ years of Clinical Research Associate experience monitoring clinical trials.
• Hands-on experience with cardiology and/or neurology therapeutic areas.
• Strong knowledge of ICH-GCP guidelines and FDA regulations.
• Experience with EDC systems, CTMS, and eTMF platforms.

Responsibilities

• Conduct site monitoring visits (on-site and remote) for cardiology or neurology trials to ensure protocol adherence and data integrity.
• Review and verify clinical data, source documents, and CRFs/eCRFs.
• Ensure patient safety through adverse event reporting and related follow-up.
• Collaborate with investigators, site staff, and cross-functional teams to support study execution.
• Identify, document, and resolve site issues, protocol deviations, and data queries.
• Assist with site initiation, interim monitoring, and close-out visits.
• Maintain TMF documentation and monitoring reports.

Skills

Attention to detail

Communication

Organizational skills

Problem-solving

Travel readiness

Education

Bachelor's degree in Life Sciences or related field

Tools

EDC

CTMS

eTMF

Job description

Piper Companies is seeking a Clinical Research Associate specializing in Cardiology or Neurology to support clinical trials within the pharmaceutical and biotechnology industry. The Clinical Research Associate role is ideal for a detail-oriented professional with experience monitoring cardiovascular or neurological studies and ensuring compliance with regulatory and protocol requirements throughout the lifecycle of the clinical trial.

Responsibilities of the Clinical Research Associate:

• Conduct site monitoring visits (on-site and remote) for cardiology or neurology clinical trials to ensure protocol adherence, GCP compliance, and data integrity.
• Review and verify clinical data, source documentation, and case report forms (CRFs/eCRFs).
• Ensure patient safety through adverse event reporting, serious adverse event follow-up, and safety documentation review.
• Collaborate with investigators, site staff, and cross-functional clinical teams to support study execution.
• Identify, document, and resolve site issues, protocol deviations, and data queries in a timely manner.
• Assist with site initiation, interim monitoring, and close-out visits.
• Maintain accurate trial master file (TMF) documentation and monitoring reports.

Requirements of the Clinical Research Associate:

• Bachelor’s degree in Life Sciences, Nursing, or a related field.
• 2+ years of Clinical Research Associate experience monitoring clinical trials.
• Hands-on experience with cardiology and/or neurology therapeutic areas.
• Strong knowledge of ICH-GCP guidelines and FDA regulations.
• Experience working with EDC systems, CTMS, and eTMF platforms.
• Ability to travel 8-10 days per month required by study needs.
• Excellent communication, organizational, and problem-solving skills.

Compensation for the Clinical Research Associate:

• $100,000 - $135,000 base salary
• Full Comprehensive Benefits: Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law.

Keywords: Clinical Research Associate, CRA, Cardiology, Neurology, Cardiovascular Clinical Trials, Neuroscience Clinical Trials, GCP, ICH-GCP, FDA Regulations, Site Monitoring, EDC, eTMF, CTMS, Clinical Operations, Pharmaceutical, Biotechnology

This job opens for applications on 9/25/2026. Applications for this job will be accepted for at least 30 days from the posting date.

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