Senior CRA I - Remote, 60-75% Travel

ZP Group; United States; Remote; USD 125,000 - 140,000; Full time

Benefits offered by this job

Medical, dental, vision benefits

401(k)

Job summary

Piper Companies is seeking a Senior Clinical Research Associate I for a remote permanent role with 60-75% travel to sites in the US. This Senior CRA I will support cardiovascular, CNS, and metabolic studies while partnering closely with investigative sites to ensure high-quality trial execution.

Responsibilities include monitoring visits, primary site contact duties, data review for accuracy, training site staff on protocol requirements, and elevating quality or compliance concerns to support

Qualifications

• 1–4 years of onsite clinical monitoring experience, aligned to CRA II or Senior CRA I level.
• Experience supporting cardiovascular, CNS, diabetes or metabolic indications.
• Strong working knowledge of GCP, ICH guidelines, and FDA regulatory requirements.
• Proficiency with CTMS and EDC systems.
• Bachelor's degree in life sciences, nursing, or related discipline; Spanish fluency preferred for Florida or Puerto Rico.

Responsibilities

• Perform routine and close-out monitoring visits to ensure studies are conducted in alignment with GCP, ICH, and applicable regulations.
• Serve as the primary point of contact for assigned research sites, fostering strong relationships and ongoing communication.
• Review site data, source documentation, and regulatory files to confirm accuracy, completeness, and protocol adherence.
• Provide guidance and training to site staff on protocol requirements, study procedures, and compliance expectations.
• Identify, document, and elevate quality or compliance concerns while supporting resolution efforts.

Skills

GCP/ICH

FDA regulations

Site monitoring

CTMS proficiency

EDC proficiency

Education

Bachelor's degree in life sciences or related

Tools

CTMS

EDC systems

Job description

Piper Companies is seeking a Senior Clinical Research Associate I for a remote permanent role with 60-75% travel to sites in the US. This Senior CRA I will support cardiovascular, CNS, and metabolic studies while partnering closely with investigative sites to ensure high-quality trial execution.

Responsibilities include monitoring visits, primary site contact duties, data review for accuracy, training site staff on protocol requirements, and elevating quality or compliance concerns to support