Field-Based Clinical Research Associate (Remote)

Piper Companies

United States

Remote

USD 110,000 - 125,000

Full time

9 days ago
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Benefits offered by this job

Medical, dental, vision
401(k)
PTO

Job summary

Piper Companies is seeking a Clinical Research Associate to support a leading pharmaceutical/biotechnology organization on the West/West Coast US. This field-based CRA role suits professionals with independent monitoring experience who excel at building relationships with investigative sites.

Responsibilities include monitoring visits, ensuring adherence to ICH-GCP, reviewing documentation, and collaborating with site staff.

Qualifications

  • 2+ years of independent monitoring experience as a Clinical Research Associate.
  • Excellent knowledge of ICH-GCP guidelines and clinical trial regulations.
  • Experience in pharmaceutical, biotechnology, or medical device studies preferred.
  • Strong communication, organization, and problem-solving skills.
  • Willingness to travel frequently, including overnight travel.

Responsibilities

  • Conduct site qualification, initiation, routine monitoring, and closeout visits.
  • Ensure studies comply with ICH-GCP, protocols, and regulatory requirements.
  • Review source documents, site records, and data for accuracy and compliance.
  • Build and maintain relationships with investigators and site staff.
  • Identify, document, and resolve site issues while supporting study execution.
  • Complete monitoring reports and follow-up documentation within timelines.
  • Travel extensively to clinical research sites as required.

Skills

Independent monitoring
Communication
Organization
Problem-solving
Travel readiness

Education

Bachelor's degree in science/healthcare

Job description

Piper Companies is seeking a Clinical Research Associate to support a leading pharmaceutical/biotechnology organization on the West/West Coast US. This field-based CRA role suits professionals with independent monitoring experience who excel at building relationships with investigative sites.

Responsibilities include monitoring visits, ensuring adherence to ICH-GCP, reviewing documentation, and collaborating with site staff.

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