Remote CRA II: Cardiovascular & CNS Trials (Travel Required)

ZP Group; United States; Remote; USD 100,000 - 125,000; Full time

Benefits offered by this job

Medical

Dental

Vision

Sick leave

401(k)

Job summary

Piper Companies is seeking a Clinical Research Associate II for a remote permanent role with substantial travel across the United States. The CRA II will support cardiovascular, CNS, and metabolic studies while partnering with investigative sites to ensure high-quality trial execution.

Responsibilities include monitoring visits, site communication, data review, and training site staff on protocol requirements and compliance.

Qualifications

• 1–4 years of onsite clinical monitoring experience, aligned to CRA II or Senior CRA I level.
• Experience supporting clinical trials within cardiovascular, CNS, diabetes, or metabolic indications.
• Strong working knowledge of GCP, ICH guidelines, and FDA regulatory requirements.
• Proficiency with CTMS, EDC systems, and standard clinical trial documentation.
• Bachelor’s degree in life sciences, nursing, or a related discipline; Spanish fluency is highly preferred for candidates based in 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.

Job description

Piper Companies is seeking a Clinical Research Associate II for a remote permanent role with substantial travel across the United States. The CRA II will support cardiovascular, CNS, and metabolic studies while partnering with investigative sites to ensure high-quality trial execution.

Responsibilities include monitoring visits, site communication, data review, and training site staff on protocol requirements and compliance.