Clinical Research Nurse

Contemporary Staffing

Ames, IAFull-time

Behavioral Health Market Context

Apply Nowvia Contemporary Staffing - Contemporary Staffing Solutions

Job Description

s of safety, accuracy, and compliance. The ideal candidate will bring strong clinical experience, excellent organizational skills, and a genuine interest in advancing healthcare through research. This is a direct-hire opportunity based in Ames, IA, with a consistent weekday schedule and no weekend or holiday work.

Compensation:

$90,000 – $95,000 annually

Work Schedule:

Monday through Friday, 8:00 a.m. – 5:00 p.m. CST (No weekends or holidays)

Key Responsibilities of the Clinical Research Nurse:
• Execute clinical trial procedures according to established study protocols, ensuring compliance with ethical standards and regulatory guidelines.
• Perform clinical and technical tasks such as venipuncture, specimen collection and processing, vital signs, injections, IV infusions, ECGs, and other study-related procedures with precision and care.
• Support participant engagement by assisting with recruitment, screening, informed consent, and providing ongoing nursing support throughout the trial process.
• Collaborate with investigators and research teams to maintain protocol accuracy, data quality, and seamless coordination between all stakeholders.
• Document and report study data accurately in accordance with Good Clinical Practice (GCP) standards and institutional requirements.

Qualifications and Skills for the Clinical Research Nurse:
• Active LPN license required; RN preferred.
• Bachelor’s degree in Nursing or related field preferred; equivalent experience considered.
• Minimum of 5 years of nursing experience, ideally within research, ER, infusion, or home health environments.
• Strong understanding of GCP standards and clinical trial regulatory processes.
• Highly organized with the ability to manage multiple studies in a fast-paced setting.
• Excellent communication and teamwork skills with a proactive, engaged approach to patient care and research collaboration.

Why Join Us?

This is a great opportunity for a dedicated nurse eager to move beyond traditional bedside care and make an impact in clinical research. You’ll enjoy regular hours, a supportive team environment, and the chance to be directly involved in advancing treatments that improve patient lives. Bring your clinical expertise to a purpose-driven setting that values precision, collaboration, and professional growth.

About Us:

Contemporary Staffing Solutions (CSS) is a trusted leader in providing contract, temporary, temp-to-hire, and direct hire staffing solutions. With decades of experience, we’ve grown from a staffing agency to a nationwide provider of workforce management solutions. Our niche recruitment expertise spans Accounting & Finance, Call Center & Office Support, Human Resources, Sales & Marketing, and Information Technology. Explore more about CSS and how we connect great talent with exceptional opportunities by visiting www.ContemporaryStaffing.com.

Qualifications

  • The ideal candidate will bring strong clinical experience, excellent organizational skills, and a genuine interest in advancing healthcare through research
  • Minimum of 5 years of nursing experience, ideally within research, ER, infusion, or home health environments
  • Strong understanding of GCP standards and clinical trial regulatory processes
  • Highly organized with the ability to manage multiple studies in a fast-paced setting
  • Excellent communication and teamwork skills with a proactive, engaged approach to patient care and research collaboration

Benefits

  • $90,000 – $95,000 annually

Responsibilities

  • This position blends hands-on nursing care with research coordination—offering the opportunity to contribute to meaningful studies while ensuring the highest standards of safety, accuracy, and compliance
  • Monday through Friday, 8:00 a.m. – 5:00 p.m. CST (No weekends or holidays)
  • Execute clinical trial procedures according to established study protocols, ensuring compliance with ethical standards and regulatory guidelines
  • Perform clinical and technical tasks such as venipuncture, specimen collection and processing, vital signs, injections, IV infusions, ECGs, and other study-related procedures with precision and care
  • Support participant engagement by assisting with recruitment, screening, informed consent, and providing ongoing nursing support throughout the trial process
  • Collaborate with investigators and research teams to maintain protocol accuracy, data quality, and seamless coordination between all stakeholders
  • Document and report study data accurately in accordance with Good Clinical Practice (GCP) standards and institutional requirements
  • You’ll enjoy regular hours, a supportive team environment, and the chance to be directly involved in advancing treatments that improve patient lives


More Jobs