Sub Investigator

Benefits

Qualifications

• •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
• •2 more items(s)

Responsibilities

• •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
• •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
• •3 more items(s)