Clinical Trials Nurse- Full Time

The Clinical Research Nurse (CRN) is responsible for coordination of research studies conducted by Mercy Research. The Clinical Research Nurse is responsible for the day-to-day operational tasks related to clinical trials and performs a variety of duties including, but not limited to, volunteer recruitment, drug/device/supply inventory maintenance, interaction with physicians, nurses, office staff, patients, and clinical monitors. Duties also include the collection, compilation, documentation and analysis of clinical research data while following local, state and federal regulations. The Clinical Research Nurse will assist in training and preceptor duties. The study load and complexity will increase from the Associate Clinical Research Nurse responsibility, thereby increasing the overall number of enrollments and visits. The Clinical Research Nurse will assist with communication and relationship building with sponsors and CROs.

Performs duties and responsibilities in a manner consistent with our mission, values, and Mercy Service Standards. Clinical Research Nurse – Oncology

Schedule: Full-Time, Day Shift

The Clinical Research Nurse (CRN) is a key member of the Mercy Research team, responsible for coordinating oncology clinical trials and ensuring compliance with all regulatory requirements. This role involves managing day-to-day operations of research studies, including patient recruitment, informed consent, data collection, and inventory control. The CRN collaborates with physicians, nurses, office staff, patients, and clinical monitors to deliver safe, efficient, and high-quality research services. Additional responsibilities include training new staff, supporting ministry-wide recruitment efforts, and building strong relationships with sponsors and CROs.

Manage patient visits efficiently, including monitoring, interviews, and diagnostic evaluations.

Maintain accurate and timely documentation in case report forms and source documents.

Prepare and process specimens for laboratory analysis.

Educate patients on drug use, disease management, and self-monitoring.

Maintain inventory of study drugs, devices, and supplies.

Participate in internal quality control and compliance monitoring.

Assist with training new staff and supporting recruitment initiatives.

Serve as a liaison with sponsors, CROs, and community partners to promote research and patient enrollment.

Attend investigator meetings and training sessions as required (may involve travel).

Contribute to a collaborative and organized research office environment.

Nursing Diploma, Associate’s Degree in Nursing, or Bachelor’s Degree in Nursing.

• Registered Nurse with a valid license in the state of practice.
• 2 years of nursing experience for candidates with a Bachelor’s degree.
• 3 years of nursing experience for candidates with an Associate’s degree or diploma program.
• vital signs, spirometry, ECGs, phlebotomy, blood glucose monitoring) or willingness to learn.

Excellent communication skills, especially in face-to-face interactions with healthcare professionals and patients.

Ability to interact respectfully and assertively with health professionals.

Working knowledge of computer applications, including Internet and Microsoft Office Suite.

Phlebotomy experience.

At least 2 years of clinical research experience.

From day one, Mercy offers outstanding benefits - including medical, dental, and vision coverage, paid time off, tuition support, and matched retirement plans for team members working 32+ hours per pay period.

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