Registered Nurse - Clinical Research

The VIOS Clinic; Creve Coeur (MO); On-site; USD 75,000 - 110,000; Full time

Job summary

The VIOS Clinic is seeking a Clinical Research Nurse to support and coordinate clinical trials within a healthcare setting in Creve Coeur, MO. You will manage protocols, ensure regulatory compliance, obtain informed consent, and accurately document trial data while delivering compassionate participant care.

The role requires RN background with trial experience and strong teamwork with physicians and research teams to uphold participant safety and data quality.

Qualifications

• RN with clinical trial support experience.
• Strong understanding of informed consent and regulatory expectations.
• Excellent documentation and data integrity skills.
• Effective communication and teamwork in multidisciplinary settings.
• Empathetic approach focused on participant safety.

Responsibilities

• Manage study protocols and ensure adherence to trial requirements.
• Maintain regulatory compliance and related documentation.
• Obtain informed consent and support participant understanding.
• Collect, verify, and document clinical research data.
• Provide compassionate, patient-centered care to research participants.
• Collaborate with physicians, research coordinators, and multidisciplinary teams across specialties.

Skills

Regulatory compliance

Informed consent

Data management

Teamwork

Patient safety

Education

RN (Registered Nurse)

Job description

Clinical Research Nurse to support and coordinate clinical trials within a healthcare and medical services environment.

Key Responsibilities

• Manage study protocols and ensure adherence to trial requirements.
• Maintain regulatory compliance and related documentation.
• Obtain informed consent and support participant understanding.
• Collect, verify, and accurately document clinical research data.
• Provide compassionate, patient-centered care to research participants.
• Collaborate with physicians, research coordinators, and multidisciplinary teams across specialties.

Qualifications & Skills

• Registered nursing background with clinical trial support experience.
• Strong knowledge of informed consent and regulatory expectations.
• Excellent documentation, data integrity, and attention to detail.
• Effective communication and teamwork skills in a multidisciplinary setting.
• Empathetic approach and commitment to participant safety and welfare.