Clinical Research Nurse

Responsibilities

• Independently coordinate and execute Phase I-III clinical research studies under the direction of the Principal Investigator.
• Manage complex interventional trials and ensure study activities are completed accurately, efficiently, and in accordance with protocol requirements.
• Screen and assess patients for eligibility, conduct informed consent discussions, and coordinate protocol-specific procedures.
• Review clinical and diagnostic information and ensure accurate documentation of study data.
• Identify, document, report, and follow up on adverse events and other safety concerns.
• Manage investigational products, including receipt, storage, dispensing, inventory, documentation, and disposition.
• Maintain accurate research records and ensure data is complete, accurate, and consistent with source documentation.
• Support IRB/IEC submissions, regulatory documentation, monitoring visits, and follow-up activities.
• Identify potential protocol deviations and work with study leadership to address compliance issues and corrective actions.
• Assist with study budgets, research billing, and financial tracking as needed.
• Maintain compliance with GCP, ICH, FDA, and applicable regulatory requirements.

Required Qualifications

• Active RN license.
• Clinical research experience, preferably with interventional trials.
• Strong understanding of GCP/ICH/FDA requirements and clinical research regulations.
• Experience with patient screening, informed consent, adverse event reporting, investigational products, and research documentation.
• Ability to independently manage competing priorities and work effectively in a fast-paced research environment.
• Strong attention to detail, critical thinking, organization, and communication skills.
• Proficiency with Microsoft Office.

Preferred

• Oncology clinical research or oncology nursing experience.
• Experience with EMR systems.
• Experience with EDC and/or CTMS platforms.
• Prior experience working with complex Phase I-III trials.

Schedule

• Monday-Friday
• 8:00 AM-5:00 PM

For California Applicants:

We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO) , and the California Fair Chance Act (CFCA).

This position is subject to a background check based on its job duties, which may include patient care, working with vulnerable populations, access to financial and confidential information, driving, working with heavy machinery, or working in a warehouse or laboratory environment. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.

Here at Medix, we are dedicated to providing workforce solutions to clients throughout multiple industries. We have been named among the Best and Brightest Companies to Work For in the Nation for two consecutive years. Medix has also been ranked as one of the fastest growing companies by Inc. Magazine.

Our commitment to our core purpose of positively impacting 20,000 lives affects not only the way we interact with our clients and talent, but also with our co-workers! The goal is lofty, but it is made attainable through the hard work and dedication of our teams and their willingness to lock arms together. Are you ready to lock arms with us?