Clinical Research Associate - 174832 - 175212

Piper Companies; United States; Remote; USD 110,000 - 125,000; Full time

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 organization within the pharmaceutical/biotechnology industry located within the West or West Coast of the United States. The Clinical Research Associate role is ideal for a clinical research professional with independent monitoring experience who thrives in a field-based environment and enjoys building strong relationships with investigative sites.

Responsibilities of the Clinical Research Associate

• Conduct site qualification, initiation, routine monitoring, and closeout visits.


• Ensure studies are conducted in compliance with ICH-GCP guidelines, protocols, and regulatory requirements.


• Review source documentation, site records, and data for accuracy and compliance.


• Build and maintain strong relationships with investigators and site staff.


• Identify, document, and resolve site issues while supporting overall study execution.


• Complete monitoring reports and follow-up documentation within required timelines.


• Travel extensively to clinical research sites as required.

Qualifications of the Clinical Research Associate

• 2+ years of independent monitoring experience as a Clinical Research Associate.


• Bachelor's degree in a scientific, healthcare, or related field preferred.


• Strong knowledge of ICH-GCP guidelines and clinical trial regulations.


• Experience within pharmaceutical, biotechnology, or medical device studies preferred.


• Excellent communication, organization, and problem-solving skills.


• Ability and willingness to travel frequently, including overnight travel.

Compensation for the Clinical Research Associate includes

• Pay Rate: 110k-125k/year


• Comprehensive benefits package including medical, dental, vision, 401(k), and PTO


• Direct-hire opportunity with long-term career growth

Application Period

This job opens for applications on 10/05/2026. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: Clinical Research Associate, CRA, CRA II, Senior CRA, Clinical Monitoring, Independent Monitoring, Site Management, Site Qualification Visits (SQV), Site Initiation Visits (SIV), Interim Monitoring Visits (IMV), Closeout Visits (COV), ICH-GCP, FDA Regulations, Clinical Trials, Oncology, Hematology, General Medicine, Vaccines, Medical Devices, Cardiovascular Studies, Pharmaceutical Research, Biotechnology, CRO, Sponsor Studies, Regulatory Compliance, Source Data Verification (SDV), Investigator Sites, Clinical Operations, Patient Safety, Protocol Compliance, Trial Master File (TMF), Veeva Vault, Risk-Based Monitoring, Field-Based CRA, Remote Monitoring, Clinical Site Management, Study Startup, Study Conduct, Clinical Research, Life Sciences, Bachelor's Degree, Travel Required, Direct Hire.

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