Remote CRA - Cardiovascular & CNS Clinical Trials (Travel)

Piper Companies; United States; Remote; USD 100,000 - 120,000; Full time

Benefits offered by this job

Health

Vision

Dental

PTO

Paid holidays and sick leave

Job summary

Piper Companies is actively seeking a CRA to join a CRO supporting global clinical programs. The CRA will oversee on-site activities to ensure GCP/ICH compliance, data integrity, and patient safety across cardiovascular, CNS, diabetes, and GLP-1 trials.

This is a fully remote position with travel within the United States. You will partner with investigators and sponsors, drive site activation and patient recruitment, provide protocol training, monitor study performance, and help manage TMF/ISF

Qualifications

• Bachelor’s degree in Life Sciences, Healthcare, Nursing, Pharmacy, or related field preferred.
• Minimum 3 years of on-site clinical monitoring experience in multiple therapeutic areas.
• Strong knowledge of GCP, ICH guidelines, and FDA regulations.

Responsibilities

• Conduct site selection, initiation, monitoring, and close-out visits for cardiovascular, CNS, diabetes, and GLP-1 trials.
• Partner with investigative sites to drive patient recruitment, enrollment, and retention strategies.
• Provide protocol-specific training and ongoing support to site personnel and maintain effective communication.
• Monitor site performance and protocol compliance, identify quality concerns, and implement corrective actions.

Skills

GCP knowledge

ICH guidelines

FDA regulations

Study management

MS Office

CTMS experience

Communication skills

Education

Bachelor's degree in Life Sciences

Tools

CTMS

EDC

Job description

Piper Companies is actively seeking a CRA to join a CRO supporting global clinical programs. The CRA will oversee on-site activities to ensure GCP/ICH compliance, data integrity, and patient safety across cardiovascular, CNS, diabetes, and GLP-1 trials.

This is a fully remote position with travel within the United States. You will partner with investigators and sponsors, drive site activation and patient recruitment, provide protocol training, monitor study performance, and help manage TMF/ISF