Clinical Research Associate (CRA)

Piper Companies; United States; Remote; USD 110,000 - 130,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Vision benefits

Sick leave

401K

Job summary

Piper Companies is seeking a Clinical Research Associate (CRA) for a remote permanent position supporting studies across the United States. The CRA will focus on remote source data verification (SDV), site monitoring, and ensuring data quality for IVD studies, while coordinating with investigators and study teams.

The ideal candidate has at least 2 years of SDV experience in clinical research, strong English communication, and the ability to travel for intermittent on-site visits as needed.

Qualifications

• Minimum 2 years of SDV experience in clinical research.
• Monitoring experience supporting in vitro diagnostic (IVD) trials.
• Native-level English communication skills.
• Ability to collaborate across all four U.S. time zones.
• Willingness to travel within the continental United States for intermittent on-site visits.
• CLIA Waiver training or experience is preferred.

Responsibilities

• Perform remote monitoring and SDV to ensure data accuracy and regulatory compliance.
• Review trial documentation and oversee study conduct per protocol and regulations.
• Collaborate with investigators, site staff, and internal teams to resolve data discrepancies.
• Conduct SIVs and participate in onsite visits to support milestones and quality objectives.
• Prepare monitoring reports and maintain essential study records per GCP and SOPs.

Skills

SDV experience

Remote monitoring

GCP knowledge

Regulatory compliance

Time zones coordination

Travel readiness

Education

CLIA Waiver training

Tools

CTMS

EDC

Job description

Piper Companies is seeking a Clinical Research Associate (CRA) to join an innovative organization within the clinical research industry for a remote permanent position supporting studies across the United States. The Clinical Research Associate (CRA) will play a key role in clinical trial oversight, with a primary focus on remote source data verification (SDV), site monitoring activities, and ensuring data quality across in vitro diagnostic (IVD) studies.

Responsibilities of the Clinical Research Associate include:

• Perform remote monitoring and source data verification activities to ensure study data accuracy, completeness, and regulatory compliance.
• Review clinical trial documentation and maintain oversight of study conduct in accordance with protocol requirements and industry regulations.
• Collaborate with investigators, site staff, and internal study teams to address data discrepancies and support timely query resolution.
• Conduct site initiation visits (SIVs) and participate in onsite monitoring visits when required to support study milestones and quality objectives.
• Prepare monitoring reports and maintain essential study records while ensuring adherence to GCP, SOPs, and applicable regulatory standards.

Qualifications for the Clinical Research Associate include:

• Minimum of 2 years of source data verification (SDV) experience within clinical research.
• Prior monitoring experience supporting in vitro diagnostic (IVD) clinical trials.
• Native-level English communication skills with strong written and verbal proficiency.
• Ability to support studies and collaborate across all four U.S. time zones.
• Willingness to travel within the continental United States for intermittent onsite monitoring visits and site initiation visits.
• CLIA Waiver training or experience is preferred.

Compensation for the Clinical Research Associate:

Salary Range: $110,000-$130,000/year (USD)

Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K

This job opens for applications on 10/30/26. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: clinical research, clinical trials, CRA, source data verification, SDV, IVD, in vitro diagnostics, clinical monitoring, remote monitoring, site management, GCP, ICH guidelines, regulatory compliance, study oversight, clinical operations, CTMS, EDC, data quality, query management, protocol adherence, site initiation visits, SIV, monitoring visits, CLIA waiver, study documentation, risk-based monitoring, FDA regulations, clinical study management, investigator sites, healthcare research, quality assurance.