Job Description

We are hiring for an RN or LPN to join a busy and well established clinical research network. This position is 100% onsite, clinical research experience is NOT required. Apply today!

Summary

The Research Nurse (RN) conducts and manages multiple clinical trials from start-up through study close-out in accordance with study protocols, Good Clinical Practice (GCP), and organizational Standard Operating Procedures (SOPs).

Duties / Responsibilities

• Conduct and manage clinical trials in accordance with study protocols, GCP, ICH Guidelines, and internal SOPs.
• Implement and coordinate assigned clinical trials, including start-up activities, vendor management, subject recruitment, source document development and review, scheduling participants, protocol training, regulatory document collection, conducting study visits, ensuring timely data entry and query resolution, managing and reporting adverse events, serious adverse events, and deviations, implementing protocol amendments, and completing all close-out reports.
• Apply project management principles to identify and mitigate risks while improving quality throughout study conduct.
• Develop, coordinate, and implement research and administrative strategies to successfully manage assigned protocols.
• Communicate effectively and professionally with colleagues, leadership, study participants, sponsors, CROs, and vendors.
• Maintain confidentiality of patient protected health information, sponsor confidential information, and internal organizational information.
• Verify and escalate patient safety concerns by ensuring all adverse events, serious adverse events, and events of special interest are followed and reported per protocol and SOP requirements.
• Create, collect, and submit regulatory documents to sponsors and IRBs in compliance with protocols, GCP/ICH regulations, and IRB requirements.
• Evaluate potential participants for clinical trial eligibility through phone and in-person pre-screens.
• Create and execute recruitment strategies in collaboration with the Clinical Research Team.
• Demonstrate understanding of key timelines, endpoints, required vendors, and target patient populations for each assigned protocol.
• Understand the product development life cycle and the significance of protocol design, including identification of critical data points.
• Maintain knowledge of the disease process or condition under study.
• Collaborate with the Clinical Research Team to develop a Quality Control strategy for continuous review of study work and preparation for monitoring visits.
• Perform clinical duties within the RN scope of practice (e.g., drug preparation and administration, FibroScan, phlebotomy, ECGs, lab processing).
• Perform other duties as assigned.

Benefits:

• Paid Sick Leave (Medix provides paid sick leave according to state and local sick leave ordinances)
• Health Benefits / Dental / Vision (Medix Offers 6 different health plans: 3 Major Medical Plans, 2 Fixed Indemnity Plans (Standard and Preferred), and 1 Minimum Essential Coverage (MEC) Plan. Eligibility for health benefits is based on verifying that an average of 30 hours per week during the first 4 weeks of the work assignment has been met. If you meet eligibility requirements and take action to enroll, you will be covered no earlier than 60 days into your assignment, depending on plan selection(s).)
• 401k (eligible on the first 401k open enrollment date following 6 consecutive months on assignment. 401k Open Enrollment dates are 1/1, 4/1, 7/1, and 10/1)
• Short Term Disability Insurance
• Term Life Insurance Plan

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