Sub Investigator (NP or PA-C)

Company: ALLIANCE CLINICAL LLC
Location: Los Angeles
Posted on: February 14, 2026

Job Description:

Job Description Job Description About Company: We’re people with a purpose, dedicated to advancing medical innovation and healing technology through groundbreaking research, diligent patient care and strong executive management. Our hands-on management team and medical staff are committed to rapid, efficient trials that bring life-changing drugs to market faster; our research staff brings years and years of “in the trenches” experience conducting Phase 1-4 clinical studies. And each one is dedicated to curing disease and improving individual quality of life. MISSION STATEMENT At Alliance Clinical Network, our mission is to advance 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. About the Role: The Sub Investigator (NP or PA-C) plays a critical role in supporting clinical research studies within the healthcare and social assistance sector. This position involves collaborating closely with the Principal Investigator to ensure the integrity and compliance of clinical trials, while providing expert patient care and clinical assessments. The Sub Investigator will be responsible for enrolling and monitoring study participants, collecting and documenting clinical data, and ensuring adherence to study protocols and regulatory requirements. This role demands a thorough understanding of clinical research methodologies, patient safety considerations, and ethical standards. Ultimately, the Sub Investigator contributes to advancing medical knowledge and improving patient outcomes through rigorous and ethical clinical research. Minimum Qualifications: Current and unrestricted licensure as a Nurse Practitioner (NP) or Physician Assistant-Certified (PA-C) in the United States. Experience working in clinical research or healthcare settings involving patient care and clinical assessments. Knowledge of Good Clinical Practice (GCP) guidelines and federal regulations governing clinical trials. Strong understanding of clinical trial protocols, informed consent processes, and patient safety monitoring. Excellent communication skills and ability to work collaboratively within multidisciplinary research teams. Preferred Qualifications: Previous experience as a Sub Investigator or Clinical Research Coordinator in clinical trials. Certification in clinical research (e.g., ACRP-CP, SOCRA) or advanced training in research methodologies. Familiarity with electronic data capture (EDC) systems and clinical trial management software. Experience in therapeutic areas relevant to ongoing clinical studies, such as oncology, cardiology, or infectious diseases. Ability to contribute to protocol development and study design discussions. Responsibilities: Assist the Principal Investigator in the conduct and oversight of clinical trials, ensuring compliance with study protocols and regulatory guidelines. Perform patient assessments, including medical history reviews, physical examinations, and evaluation of adverse events related to the study. Enroll eligible participants into clinical studies and obtain informed consent in accordance with ethical standards. Document clinical data accurately and timely in case report forms and electronic data capture systems. Collaborate with research coordinators, sponsors, and regulatory bodies to facilitate smooth study operations and audits. Monitor patient safety throughout the study and report any safety concerns or protocol deviations promptly. Participate in investigator meetings, training sessions, and continuous education to stay current with clinical research best practices. Skills: The Sub Investigator utilizes clinical expertise to conduct thorough patient assessments and ensure accurate data collection, which is essential for the validity of clinical trials. Strong organizational skills are applied daily to manage multiple study participants and maintain compliance with complex protocols. Effective communication skills facilitate collaboration with the Principal Investigator, research staff, and regulatory agencies, ensuring smooth study operations and patient safety. Analytical skills are employed to identify and report adverse events or protocol deviations promptly, safeguarding participant well-being. Additionally, proficiency with clinical research software and electronic data capture tools enhances efficiency and accuracy in documentation and reporting. Benefits: 401 (k) Retirement Plan, Medical, Dental, and Vision Insurance, Paid Time Off (PTO), Floating Holidays And more!

Keywords: ALLIANCE CLINICAL LLC, Escondido , Sub Investigator (NP or PA-C), Healthcare , Los Angeles, California