Clinical Research Associate II

Piper Companies; United States; On-site; USD 100,000 - 110,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

401(k)

Job summary

Piper Companies is seeking a Clinical Research Associate II for a remote role with 60-75% travel across the United States. The CRA II will be vital in supporting cardiovascular, CNS, and metabolic studies while collaborating with investigative sites. Ideal candidates should have 1–4 years of monitoring experience, a strong understanding of GCP and ICH guidelines, and a relevant bachelor's degree. Competitive compensation includes a salary range of $100,000–$110,000/year, plus comprehensive benefits.

Qualifications

• 1–4 years of onsite clinical monitoring experience, aligned to CRA II or Senior CRA I level.
• Strong working knowledge of GCP, ICH guidelines, and FDA regulatory requirements.
• Proficiency with CTMS, EDC systems, and standard clinical trial documentation.

Responsibilities

• Perform routine and close-out monitoring visits.
• Serve as the primary point of contact for assigned research sites.
• Provide guidance and training to site staff on protocol requirements.

Skills

Clinical Monitoring

GCP and ICH Guidelines

Site Management

Data Review

Education

Bachelor’s degree in life sciences, nursing, or related discipline

Tools

CTMS

EDC systems

Job description

Piper Companies is seeking a Clinical Research Associate II to join a global organization within the clinical research and life sciences industry for a remote permanent role with 60-75% travel across the United States. This CRA II will support cardiovascular, CNS, and metabolic studies while partnering closely with investigative sites to ensure high-quality trial execution.

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.

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.

Compensation

• Salary Range: $100,000–$110,000/year (USD)
• Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401(k)

This job opens for applications on 5/11/26. Applications for this job will be accepted for at least 30 days from the posting date.