Clinical Trial Sub Investigator

Job Description

Company Description ARENSIA Exploratory Medicine is a German clinical research company specializing in early-phase clinical trials (Phase IB, IIA, Proof of Concept) with novel compounds across diverse patient populations. The company operates advanced clinics in the U.S. (Phoenix, AZ), Romania, Moldova, Georgia, Ukraine, and Bulgaria, providing patients with early access to innovative therapies in a safe and comfortable environment. With dedicated infrastructure and optimized recruitment processes, ARENSIA significantly reduces trial timelines and overall study costs compared to traditional sites. The organization is a trusted partner for leading pharmaceutical, biotech, and CRO companies, with a high rate of returning collaborators. ARENSIA was founded in 2010, and its Phoenix, AZ clinic began operations in late 2023; for questions, candidates may contact View email address on ziprecruiter.com.

Role Description The Clinical Trial Sub Investigator is a full-time, on-site role based at ARENSIA’s clinic in Phoenix, AZ. This role supports the Principal Investigator in the conduct of early-phase clinical trials, including performing protocol-specific medical assessments, documenting clinical findings, and ensuring adherence to study protocols and regulatory requirements. Daily responsibilities include reviewing and assessing potential participants for eligibility, obtaining and documenting informed consent, overseeing study visits, and monitoring participant safety through continuous clinical evaluation. The Sub Investigator collaborates closely with the clinical and research staff to ensure accurate data collection, timely reporting of adverse events, and high-quality source documentation. The role also involves participating in investigator meetings, maintaining up-to-date knowledge of study protocols and relevant therapeutic areas, and contributing to continuous improvement of site processes and patient experience.

Qualifications

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• Clinical practice skills, including taking medical histories, performing focused physical examinations, and interpreting clinical data.
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• Knowledge of Good Clinical Practice (GCP), ICH guidelines, and relevant FDA regulations, with the ability to apply these in daily trial conduct.
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• Experience in conducting or supporting clinical trials, preferably in early-phase or exploratory medicine settings.
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• Strong documentation and data review skills to ensure accurate source records, case report forms, and timely reporting of safety events.
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• Effective communication and teamwork skills to collaborate with investigators, study coordinators, nurses, and external partners.
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• Ability to manage multiple studies and patient visits, prioritize tasks, and maintain high attention to detail in a fast-paced environment.
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• Professional degree (NP or PA) with an active, unrestricted license to practice in Arizona
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• Prior experience in a research unit, hospital, or outpatient setting; experience with Phase I or Phase II trials is an advantage.
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