Sub Investigator (NP or PA-C)

JOB LOCATION/SCHEDULE: Monday – Friday / on-site / Las Vegas, NV

COMPANY OVERVIEW: At Alliance Clinical Network we’re people with a purpose, dedicated to advancing medical innovation and healing technology through groundbreaking research. We bring our energy and our passion to improving patient lives every day.

SUMMARY: The Sub-Investigator supports the Investigator MD in conducting clinical research studies, ensuring compliance with protocols, GCP guidelines, and regulatory requirements. Responsibilities include reviewing subject medical histories, providing medical oversight for study procedures, making medical decisions, and maintaining accurate documentation in eSource. The role requires strict adherence to confidentiality and study protocols while meeting all deadlines and requirements.

ESSENTIAL DUTIES AND RESPONSIBILITIES

• Comply with all company policies, procedures, and conduct.
• Strictly adhere to confidentiality and compliance standards.
• Review medical histories and concomitant medications of study subjects.
• Confirm inclusion and exclusion study criteria.
• Field subject questions related to the investigational product, study procedures and health.
• Provide medical oversight required for medically attended events such as vaccinations and infusions.
• Maintain GCP and study specific training requirements.
• Oversee aspects of clinical trials as directed by the site Investigator MD.
• Perform clinical study-related procedures.
• Make medical judgements and other decisions on behalf of the Investigator MD.
• Meet all study protocol requirements and deadlines.
• Perform accurate and timely documentation in eSource.
• Assist in answering queries and documentation in eSource.

QUALIFICATION REQUIREMENTS:

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

EDUCATION AND EXPREIENCE:

• Bachelor’s Degree or higher degree in medical or science related field (MD, DO, NP, PA, etc.) required.
• Previous experience in clinical research, preferably in a Sub-Investigator or similar role.
• Strong knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
• Familiarity with clinical trial protocols, medical histories, and study procedures.
• Experience with clinical documentation, including eSource systems, is preferred.
• Excellent communication and interpersonal skills, with the ability to interact with study participants and research teams effectively.
• Ability to make medical decisions and provide oversight within the scope of the study.