Clinical Research Nurse

Careers at Rovia

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Saint Charles, MO Until 10/3/2026 First posted August 4, 2026 Last posted August 4, 2026
Job description

About Us

At Rovia Clinical Research, we’re on a mission to bring innovative treatments to patients, improving the health and lives of our local patient communities. We believe in building a workplace where people feel supported, valued, and excited to grow their careers. Whether you’re just starting out or looking for a new path, you’ll be part of a team that truly works together and makes an impact. Our team is driven by our core values: People First, Humility, Integrity, One Team, and Results Accountability.




Position Summary:

The Clinical Research Nurse is responsible for coordinating and executing clinical trials in accordance with study protocols, ICH/GCP guidelines, sponsor requirements, and Rovia SOPs. This role partners closely with site teams to support study startup, enrollment, data quality, and overall study success. No experience in clinical research required!

 

Key Responsibilities:

  • Conducts and coordinates patient visits in accordance with study protocols.
  • Performs clinical tasks such as vital signs, EKGs, specimen collection and processing, and phlebotomy as applicable.
  • Ensures informed consent is properly obtained and documented.
  • Educates and guides participants through the study, ensuring a positive patient experience.
  • Monitors subject safety, reports adverse events, and escalates concerns as appropriate.
  • Completes timely and accurate source documentation and EDC data entry.
  • Resolves data queries and ensures data integrity.
  • Maintains investigational product accountability and proper storage and handling.
  • Prepares for and supports monitoring visits, audits, and inspections.
  • Collaborates with site staff and investigators to ensure protocol adherence and efficient visit flow.
  • Perform other duties as assigned.

Skills/Abilities:

  • Strong knowledge of medical terminology and clinical procedures.
  • Understanding of ICH/GCP and regulatory requirements.
  • Excellent organizational skills and attention to detail.
  • Strong interpersonal and patient-facing communication skills.
  • Ability to multitask and manage competing priorities in a fast-paced environment.
  • Proficiency in Microsoft Office, EDC, and CTMS applications.
  • Ability to work both independently and collaboratively.
  • High level of professionalism and commitment to patient confidentiality.

Education/Experience:

  • Current RN or LPN licensure required.
  • Experience with phlebotomy and vital signs required.

Position will require availability to start at 6:00AM.

About this role

Summary

Coordinate clinical trials, perform medical procedures, ensure protocol adherence, support data collection.

Job title

Clinical Research Nurse

Experience level

entry level

Industry

healthcare

Location requirements

Must be in Saint Charles, MO, no remote work allowed.

Salary

Not specified

Management role

No

Skills & keywords

Required skills

medical terminologyclinical proceduresICH/GCPregulatory requirementsorganizationcommunicationproficiency in Microsoft OfficeEDCCTMS

Preferred skills

None specified

Specializations

clinical proceduresregulatory requirementspatient care
Locations

Structured locations inferred from the posting.

St Charles, MO, USA

On-site City