Senior Clinical Research Associate - 177467

Piper Companies; United States; Remote; USD 125,000 - 140,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Sick leave (as required by law)

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 across the United States. The Senior CRA I will monitor cardiovascular, CNS, and metabolic studies, collaborating closely with investigative sites to ensure high-quality trial execution.

The role requires 1–4 years of onsite monitoring experience and a strong working knowledge of GCP/ICH and FDA regulations.

Qualifications

• 1–4 years of onsite clinical monitoring experience.
• Experience supporting trials in cardiovascular, CNS, diabetes, or metabolic indications.
• Strong knowledge of GCP, ICH guidelines, and FDA regulations.
• Proficiency with CTMS, EDC systems, and standard trial documentation.
• Bachelor’s degree in life sciences or nursing; Spanish fluency preferred for candidates based in Florida or Puerto Rico.

Responsibilities

• Perform routine and close-out monitoring visits ensuring studies align with GCP/ICH and regulations.
• Serve as primary site contact, fostering relationships and ongoing communication.
• Review site data, source documents, and regulatory files for accuracy and protocol adherence.
• Provide guidance and training to site staff on protocol requirements and study procedures.
• Identify, document, and escalate quality or compliance concerns and support resolution.

Skills

Site monitoring

GCP knowledge

ICH guidelines

FDA regulations

CTMS

EDC systems

Regulatory compliance

Site communication

Education

Bachelor’s in life sciences

Nursing

Tools

CTMS

EDC systems

Job description

Piper Companies is seeking a Senior Clinical Research Associate I to join a global organization within the clinical research and life sciences industry 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 of the Senior Clinical Research Associate I include:

• 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 escalated quality or compliance concerns while supporting resolution efforts.

Qualifications for the Senior Clinical Research Associate I include:

• 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 for the Senior Clinical Research Associate I:

Salary Range: $125,000–$140,000/year (USD)

Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401(k)

This job opens for applications on 10/30/26. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: clinical research, clinical trials, CRA, GCP, ICH, regulatory compliance, site monitoring, clinical monitoring, CTMS, EDC, cardiovascular studies, CNS trials, diabetes research, GLP-1, site management, FDA regulations, clinical operations, documentation, quality assurance, protocol compliance, investigator sites, patient safety, clinical development.

#LI-MB1 #LI-REMOTE