Clinical Research Associate - 170044

Piper Companies; United States; Remote; USD 100,000 - 140,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Vision benefits

401K

Job summary

Piper Companies is seeking a Clinical Research Associate (CRA) to support a leading organization within the clinical research industry across the United States. The CRA will provide site management and monitoring support for clinical trials in Oncology, Cardiovascular, GLP-1/Obesity, Diabetes, or Ophthalmology research programs.

Multiple openings are available. This role involves onsite and remote monitoring, site activation, and data review to ensure protocol compliance and patient safety.

Qualifications

• Bachelor's degree in Life Sciences or related field required.
• 2+ years of clinical monitoring experience in pharma/CRO.
• Experience across Oncology, Cardiovascular, GLP-1/Obesity, Diabetes, Ophthalmology or related areas preferred.

Responsibilities

• Conduct onsite and remote monitoring to evaluate study progress, safety, and protocol compliance.
• Lead site activation, investigator training, and start-up readiness assessments.
• Review data, source docs, and regulatory records for accuracy and completeness.
• Collaborate with investigative sites and internal teams to address findings and maintain timelines.
• Support ongoing oversight of trials through routine travel and monitoring visits.

Skills

Clinical monitoring

Regulatory compliance

Communication skills

Project coordination

Education

Bachelor's degree in Life Sciences

Tools

EDC platforms

CTMS

Job description

Piper Companies is seeking a Clinical Research Associate (CRA) to support a leading organization within the clinical research industry across the United States. The Clinical Research Associate (CRA) will provide site management and monitoring support for clinical trials within Oncology, Cardiovascular, GLP-1/Obesity, Diabetes, or Ophthalmology research programs. Multiple openings are available, and candidates may specialize in one or more therapeutic areas.

Responsibilities of the Clinical Research Associate (CRA):

• Conduct onsite and remote monitoring activities to evaluate study progress, participant safety, and protocol compliance.
• Lead site activation efforts, including investigator training and study start-up readiness assessments.
• Review clinical data, source documentation, and regulatory records to ensure accuracy and completeness.
• Partner with investigative sites and internal study teams to address findings, resolve issues, and maintain study timelines.
• Support ongoing oversight of clinical trials through routine travel, monitoring visits, and site relationship management.

Qualifications of the Clinical Research Associate (CRA):

• Bachelor's degree in Life Sciences, Nursing, Healthcare, or a related scientific field.
• 2+ years of clinical monitoring experience within a pharmaceutical, biotechnology, CRO, or clinical research environment.
• Experience supporting studies in Oncology, Cardiovascular, GLP-1/Obesity, Diabetes, Ophthalmology, or other related therapeutic areas. Experience in all therapeutic areas is not required.
• Working knowledge of EDC platforms, CTMS applications, and clinical trial technologies.
• Strong understanding of ICH-GCP guidelines, regulatory requirements, and clinical research best practices with excellent communication and organizational skills.

Compensation of the Clinical Research Associate (CRA):

• Salary Range: $100,000 - $140,000 dependent on experience
• Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K

This job opens for applications on 9/4/26. Applications for this job will be accepted for at least 30 days from the posting date.