Remote Clinical Research Associate | Travel-Ready CRA

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

Benefits offered by this job

Medical, dental, vision

401(k)

PTO

Direct-hire opportunity

Job summary

Piper Companies seeks a Clinical Research Associate to support a leading organization within the pharmaceutical/biotechnology industry, located on the West Coast of the United States. Responsibilities include site qualification, initiation, monitoring, and closeout visits while ensuring compliance with ICH-GCP, protocols, and regulatory requirements.

The role involves data review, strong investigator relationships, issue resolution, and extensive travel as needed.

Qualifications

• 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.

Responsibilities

• 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.

Skills

Independent monitoring experience

Communication

Travel willingness

Regulatory knowledge

Education

Bachelor's degree in science/healthcare

Tools

Veeva Vault

TMF

Job description

Piper Companies seeks a Clinical Research Associate to support a leading organization within the pharmaceutical/biotechnology industry, located on the West Coast of the United States. Responsibilities include site qualification, initiation, monitoring, and closeout visits while ensuring compliance with ICH-GCP, protocols, and regulatory requirements.

The role involves data review, strong investigator relationships, issue resolution, and extensive travel as needed.