Clinical Research Regulatory Nurse Job at BVL Clinical Research, Liberty, MO

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  • BVL Clinical Research
  • Liberty, MO

Job Description

BVL Clinical Research | Liberty, MO | Monday–Friday, 8:00AM - 4:30PM (on-site)

ABOUT

BVL Clinical Research is a dedicated research site in Liberty, Missouri, focused on advancing treatments for gastroenterology and inflammatory bowel disease (IBD). We conduct clinical trials for Crohn’s disease and ulcerative colitis with a strong emphasis on patient safety, education, and high-quality care.

OVERVIEW

We are seeking a Registered Nurse (RN) to join our on-site clinical research team. This full-time role is ideal for an RN looking to transition from shift-based care into a Monday–Friday schedule while continuing hands-on patient care.

You’ll work directly with patients participating in clinical trials, combining nursing care with research coordination to ensure safe study visits, clear communication, and regulatory-quality documentation. This position supports higher-acuity studies and maintains active clinical skills such as IV therapy, infusions, injections, and close safety monitoring.

You’ll collaborate closely with the Principal Investigator, Director of Operations, and study team to support patient safety, protocol adherence, and a positive research experience.

LOCATION AND SCHEDULE

Location: This is a FULLY ON-SITE position in Liberty, Missouri.

Candidates must currently live within commuting distance of Liberty, MO to be considered. Relocation assistance is not available, and we are unable to consider candidates planning to relocate independently.

Schedule: Primarily Monday–Friday, 8:00 AM–4:30 PM, with occasional flexibility to support patient schedules or monitoring visits. Advance notice will be provided whenever possible.

KEY RESPONSIBILITIES

Patient Care & Research Nursing

  • Provide direct patient care during study visits, including IV therapy, infusions, injections, and nursing assessments
  • Monitor patients closely before, during, and after procedures to ensure safety and comfort
  • Educate patients and families about study procedures, expectations, and follow-up requirements
  • Support the informed consent process and patient screening activities
  • Collect, process, and ship blood and laboratory specimens per protocol
  • Document care accurately and promptly; escalate safety concerns or adverse events to the PI

Clinical Research & Regulatory Coordination

  • Ensure study activities follow approved protocols, GCP, and site procedures
  • Maintain study documentation and regulatory files
  • Support IRB submissions, study start-up, monitoring visits, and inspection readiness
  • Assist with safety reporting, protocol deviations, and data quality activities

Operations & Team Support

  • Help develop study visit guides, workflows, and training tools
  • Track staff training and study readiness requirements
  • Prepare basic study status summaries (e.g., enrollment, visit activity)
  • Coordinate across team members to keep studies on track

As Needed

  • Assist with biohazard specimen shipping (training provided if required)
  • Support study closeout activities and document retention requirements

QUALIFICATIONS

Required

  • Active, unencumbered Missouri RN license
  • Strong patient communication and documentation skills
  • Comfort working independently and as part of a multidisciplinary team

Preferred

  • Associate or Bachelor’s degree in Nursing preferred; related health science degrees considered with active RN licensure.
  • Minimum 5 years of healthcare experience
  • Clinical research experience
  • Familiarity with ICH-GCP and FDA-regulated studies
  • Experience with IV therapy and higher-acuity patient monitoring
  • Experience with EDC/CTMS systems
  • BLS/ACLS (protocol dependent)

COMPENSATION & BENEFITS

Compensation for this role is based on relevant experience, clinical research background, and protocol acuity. We are open to discussion with well-qualified candidates.

Benefits include paid time off (PTO), paid holidays, and access to medical, dental, and vision insurance.

At BVL, you’ll join a collaborative and supportive team dedicated to advancing care for patients with gastrointestinal conditions. We value high-quality research, thoughtful teamwork, and a strong commitment to patient safety.

As a growing private research site, we offer:

  • Hands-on involvement in innovative clinical trials
  • Opportunities to grow in clinical research, regulatory work, and site operations
  • A team culture where your expertise, ideas, and contributions are genuinely valued

If you’re looking to apply your nursing skills in a research-focused environment while continuing to grow professionally, we’d like to hear from you!

Learn more at BVLResearch.com

BVL Clinical Research is an equal opportunity employer. This job description may be modified at any time to meet operational needs, consistent with applicable laws and regulations.

Job Tags

Full time, Relocation, Relocation package, Monday to Friday, Shift work

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