Remote Cardiology CRA - Lead Monitoring & Data Integrity

Piper Companies

United States

Remote

USD 100,000 - 130,000

Full time

4 days ago
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Benefits offered by this job

Health benefits
Vision benefits
Dental benefits
Paid time off (PTO)
Paid holidays and sick leave as law

Job summary

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 CRA will monitor trials, ensure data integrity, and support investigative sites in compliance with regulatory standards and study protocols.

Responsibilities include site visits, data review, discrepancy resolution, and collaboration with investigators and sponsors to drive study success.

Qualifications

  • Bachelor’s degree in Life Sciences, Nursing, or related field.
  • 2+ years of clinical research monitoring experience.
  • Strong knowledge of ICH-GCP guidelines and FDA regulations.
  • Experience with EDC systems and CTMS.

Responsibilities

  • 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 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.

Skills

Organizational skills
Communication skills
Problem-solving

Education

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

Tools

EDC systems
CTMS / clinical trial management tools

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 CRA will monitor trials, ensure data integrity, and support investigative sites in compliance with regulatory standards and study protocols.

Responsibilities include site visits, data review, discrepancy resolution, and collaboration with investigators and sponsors to drive study success.

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