Sub Investigator (NP or PA-C)

ALLIANCE CLINICAL LLC • Los Angeles, CA

16d

About The Position

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.

Requirements

• 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.

Nice To Haves

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: No Education Listed