Clinical Research Coordinator

ABOUT

BVL Clinical Research is a premier clinical research site specializing in gastroenterology and inflammatory bowel disease (IBD) studies. Our team partners with leading physicians, sponsors, and patients to advance innovative treatments that improve lives.

Due to increased study volume, we're seeking a Clinical Research Coordinator (CRC) to join our on-site team in Liberty, Missouri. This position is ideal for candidates with a background in healthcare or research who want to play a hands-on role in the development of new medical therapies.

PLEASE NOTE:

We are only considering LOCAL CANDIDATES at this time. Due to hiring timelines, applicants must already be located in a commutable distance to Liberty, MO. Relocation assistance is not offered, and self-relocating candidates will not be considered.

POSITION OVERVIEW

As a CRC, you'll work under the direction of the Principal Investigator (PI) to coordinate and manage all aspects of clinical trial operations. You'll collaborate with patients, physicians, sponsors, and research staff to ensure studies are conducted with accuracy, safety, and full regulatory compliance.

This position blends hands-on patient care with the opportunity to help advance innovative new treatments.

RN license is preferred but not required. We also welcome candidates with relevant clinical, laboratory, or research coordination experience who do not hold an RN license. Experience with Phase 2–4 clinical trials is a strong plus.

The CRC role is a hands-on, patient-facing position that requires comfort with direct patient interaction as well as paper documentation, physical binder-based record keeping on site, and select electronic systems within a smaller team environment.

SCHEDULE

Our standard hours are Monday–Friday, 8:00 AM–4:30 PM (in-person).

This role may infrequently require work outside of these hours, only as needed for sponsor/CRO visits or specific study deadlines. Advance notice will be provided whenever possible.

Key Responsibilities

• Explain study protocols, procedures, and treatments to patients and families
• Conduct the informed consent process in collaboration with investigators
• Prepare and process laboratory specimens; ship frozen samples per study protocol
• Manage study documentation, including case report forms and regulatory files
• Monitor, document, and report adverse events to the IRB and sponsors
• Ensure compliance with all study protocols and regulatory standards
• Coordinate subject screening, enrollment, and follow-up visits
• Assist with feasibility assessments and pre-study/site initiation visits
• Maintain study data integrity and implement quality control procedures
• Collaborate with PIs, sponsors, and monitors to support study execution
• Participate in audits, investigator meetings, and training sessions
• Support preparation of study reports and internal communications
• Perform other assigned duties and comply with all BVL Research policies and standards

Education

• Bachelor's degree in a health-related field (Nursing, Life Sciences, or equivalent)

Preferred Experience & Qualifications

• 2+ years of experience in clinical research coordination, nursing, or healthcare
• Familiarity with Phase 2, 3, or 4 clinical studies
• Knowledge of FDA, GCP, and clinical trial regulatory requirements
• Strong attention to detail, organizational, and communication skills
• Proficiency in Microsoft Office and Google Workspace
• Active RN license (preferred but not required)

COMPENSATION & BENEFITS

Compensation is based on relevant experience and qualifications. The posted salary reflects the minimum starting rate, and 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.

Why Join BVL Clinical Research?

At BVL Clinical Research, you'll find meaningful work that helps bring new treatments to patients in need. You'll collaborate directly with physicians and research experts in a supportive, team-oriented environment while developing specialized skills in clinical research.

If you're a healthcare professional or aspiring research coordinator eager to make a real impact in advancing medical treatments, we'd love to hear from you.

Apply today to join our team and help shape the future of clinical research.

To learn more about who we are and the work we do, visit

Job Type: Full-time

Pay: From $50,000.00 per year

Benefits:

• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Vision insurance

Work Location: In person