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Weekend Clinical Trial Rn Jobs in Springfield, IL

Memorial Health

Research Nurse, Senior

Springfield, IL · On-site

$32.95 - $52.73/hr

Educates patients about clinical trial options and the risks/benefits of participating in research ... Licensure/Certification/Registry: • Illinois license to practice as Registered Nurse required ...

Memorial Health

Research Nurse, Senior

Springfield, IL · On-site

$32.95 - $52.73/hr

Educates patients about clinical trial options and the risks/benefits of participating in research ... Illinois license to practice as Registered Nurse required. Oncology certified nurse (OCN ...

Aveanna Healthcare

Registered Nurse (Rn)

IL · On-site

Days, nights, and weekend shifts- we will work with your availability! * 24/7 Local support from ... Must have and maintain an active, unencumbered license (RN) in the state in which the clinician ...

Aveanna Healthcare

Registered Nurse (Rn)

Lincoln, IL · On-site

Days, nights, and weekend shifts- we will work with your availability! * 24/7 Local support from ... Must have and maintain an active, unencumbered license (RN) in the state in which the clinician ...

Aveanna Healthcare

Registered Nurse (Rn)

Owaneco, IL · On-site

Days, nights, and weekend shifts- we will work with your availability! * 24/7 Local support from ... Must have and maintain an active, unencumbered license (RN) in the state in which the clinician ...

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All JobsWeekend Clinical Trial Rn JobsWeekend Clinical Trial Rn Jobs in Springfield, IL

Weekend Clinical Trial Rn information

See Springfield, IL salary details

$28

$61

$95

How much do weekend clinical trial rn jobs pay per hour?

As of Jul 2, 2026, the average hourly pay for weekend clinical trial rn in Springfield, IL is $61.96, according to ZipRecruiter salary data. Most workers in this role earn between $50.29 and $69.81 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Weekend Clinical Trial RN, and why are they important?

To thrive as a Weekend Clinical Trial RN, you need a current RN license, clinical nursing experience, and a solid understanding of Good Clinical Practice (GCP) guidelines. Familiarity with clinical trial management systems, electronic data capture (EDC) tools, and protocol documentation is typically required. Strong attention to detail, organizational skills, and effective communication are vital soft skills for coordinating with research teams and ensuring regulatory compliance. These skills and qualities are crucial for maintaining patient safety, data integrity, and adherence to study protocols during weekend trial operations.

What are some unique challenges of working as a Weekend Clinical Trial RN, and how can I prepare for them?

As a Weekend Clinical Trial RN, you may encounter challenges such as limited onsite support, managing urgent protocol issues, and balancing patient care with strict research timelines. Since weekends often have fewer staff members present, strong communication and problem-solving skills are essential. To prepare, familiarize yourself with study protocols in advance, establish clear lines of communication with the principal investigator and other team members, and ensure you are comfortable with electronic data capture systems. Being proactive and organized will help you provide excellent patient care while maintaining compliance with research requirements.

What are Weekend Clinical Trial RNs?

Weekend Clinical Trial RNs are registered nurses who work primarily on weekends to support clinical research studies. Their responsibilities include administering investigational treatments, monitoring patient safety, collecting data, and ensuring protocol compliance. They collaborate with research teams, patients, and other healthcare providers to facilitate trials and maintain high standards of care. This role is crucial for studies that require continuous patient oversight and data collection outside of standard weekday hours.

What is the difference between Weekend Clinical Trial Rn vs Weekend Research Nurse?

AspectWeekend Clinical Trial RnWeekend Research Nurse
CredentialsRegistered Nurse (RN) license, clinical trial trainingRegistered Nurse (RN) license, research-specific training
Work EnvironmentClinical trial sites, hospitals, research facilitiesResearch centers, hospitals, clinical research units
Employer & IndustryPharmaceutical companies, research organizationsAcademic institutions, research organizations
Work ScheduleWeekend shifts, flexible hoursWeekend shifts, flexible hours

Both roles involve RN credentials and work in research settings, often during weekends. The main difference lies in the focus: Weekend Clinical Trial Rns primarily support clinical trial protocols, while Weekend Research Nurses may be involved in broader research activities. Both roles are essential in advancing clinical research and typically require similar certifications and work environments.

What are popular job titles related to Weekend Clinical Trial Rn jobs in Springfield, IL? For Weekend Clinical Trial Rn jobs in Springfield, IL, the most frequently searched job titles are:
What job categories do people searching Weekend Clinical Trial Rn jobs in Springfield, IL look for? The top searched job categories for Weekend Clinical Trial Rn jobs in Springfield, IL are:
What cities near Springfield, IL are hiring for Weekend Clinical Trial Rn jobs? Cities near Springfield, IL with the most Weekend Clinical Trial Rn job openings:
Weekend Clinical Trial Rn jobs near you
Research Nurse, Senior

Research Nurse, Senior

Memorial Health

Springfield, IL • On-site

$32.95 - $52.73/hr

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Memorial Health rating

6.9

Company rating: 6.9 out of 10

Based on 173 frontline employees who took The Breakroom Quiz

444th of 877 rated healthcare providers

Job description

Min
USD $32.95/Hr.
Max
USD $52.73/Hr.
Overview
Works directly with cancer patients enrolled in clinical trials. Coordinates all aspects of patient care from the start of clinical trial treatment through the duration of the research study. Assists oncology physicians in the clinical management of patient treatment and outcomes. Educates patients about clinical trial options and the risks/benefits of participating in research studies. Perform data management activities for research studies (protocols).
To review Memorial's Benefits click here: Benefits - Memorial HR
Qualifications
Education:
• BSN degree preferred.
Licensure/Certification/Registry:
• Illinois license to practice as Registered Nurse required.
• Oncology certified nurse (OCN) credential or alternate certification in clinical research preferred.
Experience:
• Three years recent adult acute care experience required.
• Two years oncology nursing preferred.
• Demonstrated clinical experience appropriate to the oncology patient population; must be able to understand and coordinate the multidisciplinary nature of cancer care across settings and disease trajectory.
• Experience in research data management preferred.
Other Knowledge/Skills/Abilities:
• Excellent interpersonal skills, self-initiative, and self-responsibility required.
• Strong organizational and communication skills to manage detailed work flow
• Ability to "think outside the box" to arrive at unique solutions to patient care problems and remove barriers to care.
• Must have own transportation for frequent local travel.
• Proven ability to function in autonomous/independent role; highly motivated and self-directed.
Responsibilities
  1. Anticipates the needs of patients and their families and serves as a link between hospital departments, physician offices and outside agencies to connect patients to the resources and programs that will meet their disease and individual needs based on the research protocol.
  2. Works closely with physician offices to provide physicians, office staff, and patients a seamless entry for clinical services from the office setting to the services necessary for the patient in the research protocol.
  3. Coordinates the physician and nursing care plans between settings via personalization and customization to enhance the patient experience.
  4. Prepare and submit written adverse drug reaction reports to the NCI and research bases as required.
  5. Serve as a liaison between Memorial, the research bases, the Heartland NCORP (National Cancer Institute Community Oncology Research Program), and the individual investigators (physicians).
  6. Serve as a professional resource and/or instructor regarding clinical trials, protocol procedures, and protocol compliance for investigators, nurses, pharmacists, pathologists, radiologists, and other health care personnel both inside and outside of Memorial.
  7. Coordinates the timely scheduling of tests, procedures, appointments and treatments.
  8. Assist investigators in developing individual office systems to make protocol procedures convenient and help ensure protocol compliance.
  9. Responsible for data management activities that relate to any research studies coordinated through the Regional Cancer Center, including:
  • Patient screening and determining eligibility.
  • Obtaining informed consent and patient teaching.
  • Registering patients on research studies.
  • Clinical follow-up and data submission maintenance.
  • Quality control regarding documentation, protocol compliance, and data submission requirements.
  • Evaluations and analysis of research/data management activities.
  1. Maintain a record keeping system that documents patients registered on research studies, their protocol status, and copies of the informed consent, source documents and the data submitted.
  2. Order and monitor investigational and provided drug inventories and drug accountability records in central and satellite pharmacies.
  3. Delegate/prioritize responsibilities when appropriate due to fluctuations in workload.
  4. Attends general and site-specific cancer case conferences to identify patients who can benefit from research protocols and opportunities for Memorial to improve cancer care delivery services.
  5. Represent Memorial's Regional Cancer Center's policies and philosophy to others.
  6. Train new employees of research division in protocol coordination activities and data management.
  7. Coordinate and/or assist with clinics designed to collect research data.
  8. Coordinate and manage selected pharmaceutical trials as assigned.
  9. Promotes programs and resources of the Regional Cancer Center and Memorial Health System to patients and families, hospital departments, and physician partners.

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