Clinical Research Nurse

Job Overview:

Contemporary Staffing Solutions is seeking a Clinical Research Nurse to join our client to support ongoing clinical trials that drive medical innovation and improve patient outcomes. 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. 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.