Clinical Research Associate (Cardio) - 176577

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

Benefits offered by this job

Health, Vision, Dental

Paid Time Off

Paid Holidays

Sick Leave

Job summary

Piper Companies is seeking a Clinical Research Associate specialized in Cardiology or Neurology to support cardiovascular and neuroscience trials in the pharmaceutical and biotech industry.

The CRA will monitor sites, ensure GCP compliance, review data, and collaborate with investigators and cross-functional teams to drive study execution. Travel 8–10 days per month is required.

Qualifications

• Bachelor’s degree in Life Sciences, Nursing, or related field.
• 2+ years of CRA experience monitoring clinical trials.
• Experience in cardiology and/or neurology trials.
• Knowledge of ICH-GCP and FDA regulations.
• Proficient with EDC, CTMS and eTMF systems.
• Ability to travel 8-10 days per month.
• Excellent communication and organizational skills.

Responsibilities

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

Skills

CRA experience

Cardiology/Neurology

ICH-GCP & FDA regulations

EDC/CTMS/eTMF

Travel readiness

Communication skills

Organizational skills

Problem-solving

Education

Bachelor’s degree in Life Sciences 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 10/16/2026. Applications for this job will be accepted for at least 30 days from the posting date.

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