Clinical Research Associate (Cardio - 177214

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

Benefits offered by this job

Health benefits

Vision benefits

Dental benefits

Paid time off

Job summary

Piper Companies is seeking a Clinical Research Associate specializing in Cardiology or Neurology to support clinical trials within the pharmaceutical and biotechnology industry. The CRA role focuses on site monitoring (on-site and remote), GCP compliance, data integrity, and regulatory adherence across the trial lifecycle.

The successful candidate will hold a Bachelor's degree in Life Sciences or related field, bring 2+ years of CRA experience in cardio- or neuro-therapeutic areas, and be

Qualifications

• Bachelor's degree in Life Sciences, Nursing, or related field; required.
• 2+ years of CRA experience monitoring clinical trials.
• Experience in cardiology and/or neurology trials desirable.
• Strong knowledge of ICH-GCP and FDA regulations.
• Experience with EDC, CTMS, and eTMF platforms.

Responsibilities

• Conduct site monitoring visits (on-site and remote) ensuring protocol adherence and data integrity.
• Review and verify clinical data, source documents and case report forms.
• Ensure patient safety through adverse event reporting and safety documentation review.
• Collaborate with investigators and cross-functional teams to support study execution.
• Identify 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

Strong communication skills

Organizational skills

Problem-solving skills

Education

Bachelor’s degree in Life Sciences, Nursing, or related field

Tools

EDC systems

CTMS

eTMF platforms

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 10/26/2026. Applications for this job will be accepted for at least 30 days from the posting date.

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