Registered Nurse (Clinical Research Coordinator)

BVL Clinical Research; Liberty (MO); On-site; USD 60,000 - 80,000; Full time

Job summary

Join a leading clinical research organization as a Registered Nurse (Clinical Research Coordinator). This full-time role blends clinical care with research, offering a chance to impact future medical treatments. Candidates should possess a BSN, an active RN license in Missouri, and at least five years of experience. Responsibilities include supporting clinical trials, patient coordination, and regulatory compliance.

Benefits

Medical insurance

Vision insurance

Qualifications

• Active Registered Nurse (RN) license in Missouri required.
• Minimum of 5 years experience in healthcare operations.
• Experience with Phase I, II, and III clinical trials preferred.

Responsibilities

• Educate patients on study protocols and conduct informed consent processes.
• Coordinate patient recruitment and perform protocol-specific nursing procedures.
• Ensure compliance with regulatory standards and maintain source documents.

Skills

Deep knowledge of FDA regulations

Exceptional written and verbal communication

Strong organizational skills

Ability to interact effectively with patients

Adaptability and detail-oriented mindset

Education

Bachelor of Science in Nursing (BSN)

Tools

Microsoft Office

Google Workspace

Job description

Registered Nurse (Clinical Research Coordinator)

Registered Nurse (Clinical Research Coordinator)

1 week ago Be among the first 25 applicants

At BVL Research, we offer a unique opportunity to make a direct impact on the development of future medical treatments while maintaining work-life balance. We are seeking an experienced Registered Nurse (RN) looking to transition into a dynamic, Monday to Friday role that blends clinical care with innovative research.

This position will combine the specialized RN knowledge with the responsibilities of a Clinical Research Coordinator to create a unique opportunity.

In this role, you’ll merge your clinical knowledge with research coordination responsibilities to support and conduct clinical trials under the guidance of the Director of Operations and Principal Investigator (PI). You'll collaborate closely with patients, sponsors, physicians, and research staff to uphold the highest standards of care, compliance, and operational excellence.

• Educate patients and families on study protocols, procedures, and treatments; conduct informed consent processes with investigators.
• Prepare and ship lab specimens (including frozen and biohazardous); coordinate blood collection, processing, and infusion of study drugs per protocol.
• Screen, recruit, and coordinate patients for clinical trials; perform protocol-specific nursing procedures.
• Ensure protocol compliance by research staff; maintain source documents and regulatory files.
• Support site readiness: assist with feasibility assessments, pre-study visits, site initiation, and study monitor visits.
• Attend investigator meetings and participate in staff training; acquire continuing education relevant to research and nursing practice.
• Uphold quality and regulatory standards, including SOP compliance and agency requirements.
• Perform other assigned responsibilities as needed.

Marginal Job Duties

• Handle, package, and ship biohazardous materials in accordance with regulations.
• Assist in writing protocols and developing training tools; document and track training for study personnel.
• Support internal and external audits; help maintain data integrity and prepare research reports.
• Collaborate with the PI and Director of Operations to manage study conduct and ensure proper study closeout and secure data storage.

Qualifications & Skills

• Deep knowledge of FDA regulations and clinical research standards.
• Experience with Phase I, II, and III clinical trials and managing Investigator Site Files (ISF).
• Proficient in Microsoft Office and Google Workspace (Excel, Word, Docs, PowerPoint).
• Familiarity with clinical data systems and databases; comfortable working with medical documentation.
• Exceptional written and verbal communication, including crafting sensitive or technical documents.
• Strong organizational skills with the ability to multitask and work independently.
• Ability to interact effectively with patients, sponsors, physicians, and cross-functional teams.
• Adaptable, detail-oriented, and able to make sound decisions under pressure.

Requirements

• Registered Nurse (RN) license in Missouri (must be active and unencumbered).
• Bachelor of Science in Nursing (BSN) or an equivalent accredited degree in nursing is required.
• Minimum of 5 years of experience in healthcare operations, preferably in a clinical study environment
• Experience conducting audits, evaluations, or compliance reviews preferred.

Why Join BVL Research?

At BVL Research, you’ll play an essential role in advancing science and improving lives, while enjoying the stability of regular weekday hours. We’re committed to creating an inclusive, supportive workplace that fosters innovation.

Take the next step in your nursing career and join a research-driven organization that values your clinical knowledge and supports your growth.

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research and Science

• Industries

  Biotechnology Research and Medical Equipment Manufacturing

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Medical insurance

Vision insurance

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