What are the responsibilities and job description for the Sub Investigator position at Piper Companies?
Piper Companies is seeking a Sub Investigator to join a growing organization within the clinical research industry for an onsite permanent opportunity in Mission Viejo, California. The Sub Investigator will support ongoing and future clinical trials by providing advanced clinical oversight, subject care, and regulatory support at the site level while working closely with the Principal Investigator and research staff.
Responsibilities of the Sub Investigator include:
Salary Range: $110,000-$140,000/year (USD)
Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K
This job opens for applications on 4/16/26. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords: sub investigator, clinical research, clinical trials, advanced practice registered nurse, APRN, patient safety, protocol compliance, GCP, regulatory guidelines, informed consent, adverse event reporting, clinical documentation, site operations, healthcare research, clinical studies, medical oversight, IRB, FDA regulations, clinical operations, research nursing.
Responsibilities of the Sub Investigator include:
- Perform study-related clinical assessments and medical evaluations in accordance with approved protocols.
- Provide direct oversight of participant safety, including review of adverse events and clinical data.
- Collaborate with the Principal Investigator to ensure trials are conducted in compliance with GCP and regulatory standards.
- Support informed consent discussions and ensure subjects understand study requirements and risks.
- Contribute to protocol adherence through accurate documentation and timely clinical input.
- Master’s degree or an equivalent blend of relevant education, professional training, and hands-on experience.
- Active licensure as an Advanced Practice Registered Nurse (APRN).
- Completion of an accredited APRN program recognized by the Commission on Collegiate Nursing Education (CCNE) or the Accreditation Commission for Education in Nursing (ACEN).
- Prior experience supporting clinical research or patient care in a regulated healthcare setting.
- Strong understanding of clinical trial conduct, patient safety, and regulatory compliance.
Salary Range: $110,000-$140,000/year (USD)
Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K
This job opens for applications on 4/16/26. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords: sub investigator, clinical research, clinical trials, advanced practice registered nurse, APRN, patient safety, protocol compliance, GCP, regulatory guidelines, informed consent, adverse event reporting, clinical documentation, site operations, healthcare research, clinical studies, medical oversight, IRB, FDA regulations, clinical operations, research nursing.
Salary : $110,000 - $140,000