Sub Investigator (NP or PA-C)

Essential Duties And Responsibilities

• Assist the Principal Investigator in the design, implementation, and management of clinical research protocols.
• Conduct patient assessments, including medical history reviews, physical examinations, and monitoring of adverse events.
• Ensure compliance with all regulatory requirements, institutional policies, and Good Clinical Practice (GCP) guidelines.
• Collect, document, and maintain accurate and timely clinical trial data and source documentation.
• Collaborate with multidisciplinary teams including research coordinators, sponsors, and regulatory bodies to facilitate smooth study operations.
• Educate and communicate with study participants regarding study procedures, risks, and benefits to ensure informed consent.
• Maintain patient safety and report any safety concerns or protocol deviations promptly.
• Participate in investigator meetings, training sessions, and continuous education to stay current with clinical research standards.

Qualifications

• Experience working in clinical research or healthcare settings with direct patient care responsibilities.
• Comprehensive knowledge of clinical trial processes, regulatory requirements, and ethical standards.
• Strong understanding of medical terminology, clinical procedures, and patient assessment techniques.
• Previous experience as a Sub Investigator or Clinical Research Coordinator in a healthcare research environment, preferred.
• Familiarity with electronic data capture (EDC) systems and clinical trial management software, preferred.
• Experience working with diverse patient populations and complex clinical trial protocols, preferred.
• Strong background in a specialized therapeutic area relevant to ongoing clinical studies, preferred.
• Certificates, Licenses, And Registrations: Current and valid Nurse Practitioner (NP) or Physician Assistant-Certified (PA-C) licensure in the United States. Ability to obtain and maintain necessary certifications such as Good Clinical Practice (GCP) training. Advanced certifications related to clinical research, such as Certified Clinical Research Professional (CCRP), preferred.

About The Company

Alliance Clinical Network advances medical research by enrolling diverse populations in high-quality clinical trials. We are committed to maintaining the highest standards of integrity and excellence, and to ensuring that every participant receives respectful and compassionate care. We strive to build a tightly knit, supportive, and collaborative environment where our team members can thrive and make meaningful contributions to human health.