Clinical Research Nurse Practitioner (Sub-Investigator)

Title:

Nurse Practitoner (Sub-Investigator)

Employment Type:

Full-Time, Direct Hire, W-2 Medix is seeking a motivated and patient-focused Nurse Practitioner to join a growing clinical research team in a unique dual-function role that combines advanced clinical care responsibilities with clinical trial coordination. This opportunity is ideal for an NP with strong clinical experience who is interested in transitioning into clinical research. Prior research experience is welcomed but not required - the team is committed to providing comprehensive training, mentorship, and ongoing support to help you succeed in the role. This is an excellent opportunity to break into the clinical research industry while continuing to utilize your medical expertise in a collaborative and innovative healthcare environment. Key Responsibilities Clinical & Medical Oversight Serve as a Sub-Investigator on assigned clinical trials Perform delegated medical assessments and study-related procedures in accordance with protocol requirements Exercise sound clinical judgment to support participant safety and protocol compliance Conduct clinical procedures including phlebotomy, specimen collection, and laboratory-related duties Review and assess protocol-specific safety measures throughout study conduct Study Coordination & Trial Support Support the coordination and execution of assigned clinical studies from startup through closeout Prepare for subject visits and ensure completion of required study procedures Obtain and maintain informed consent documentation Collect and maintain accurate source documentation and study records Assist with Case Report Forms (CRFs), study tracking, and sponsor documentation Coordinate laboratory procedures, study supplies, and scheduling activities Participate in study closeout activities and operational support tasks Site Startup & Compliance Participate in Investigator Meetings and Site Initiation Visits (SIVs) Collaborate with regulatory and site teams to support study startup activities Assist with preparation and review of source documents and study materials Participate in protocol and study-specific training provided by the organization Maintain compliance with FDA regulations, GCP guidelines, and site SOPs Communication & Collaboration Serve as a point of contact for study participants and internal study teams Collaborate with investigators, coordinators, sponsors, and monitors throughout study conduct Work closely with recruitment and administrative teams to coordinate participant visits Help identify and resolve operational issues in a timely and professional manner Promote a collaborative, patient-centered, and professional research environment Qualifications Required Active Nurse Practitioner (NP) license in good standing Strong clinical experience and patient care background Experience performing medical assessments, phlebotomy, and/or clinical procedures Excellent communication, organizational, and interpersonal skills Strong attention to detail and ability to work in a fast-paced environment Interest in clinical research and willingness to learn Preferred Prior clinical research experience or exposure but not required for this position Familiarity with

GCP, FDA

regulations, or clinical trial processes Experience with documentation, patient coordination, or protocol-driven environments What We Offer Full training and mentorship in clinical research Supportive team environment with hands-on learning opportunities Opportunity to transition into and grow within the clinical research industry Exposure to innovative clinical trials and cutting-edge therapies Benefits and Competitive compensation package based on experience Schedule Full-time, 40 hours Monday - Friday, 8 AM - 5 PM If you are a clinically strong Nurse Practitioner looking to transition into clinical research, this is an outstanding opportunity to gain hands-on experience with a team dedicated to your growth and success.

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.