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Clinical Research Nurse Rn Jobs (NOW HIRING)

Medix

Clinical Research Nurse

Overland Park, KS · On-site

$38 - $42/hr

Must be a Registered Nurse (RN). * Must have BLS (Basic Life Support) and ACLS (Advanced ... Prior clinical research experience preferred. Skills * Strong organizational and communication ...

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How much do clinical research nurse rn jobs pay per hour?

As of Jul 24, 2026, the average hourly pay for clinical research nurse rn in the United States is $44.13, according to ZipRecruiter salary data. Most workers in this role earn between $36.30 and $52.40 per hour, depending on experience, location, and employer.

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

To thrive as a Clinical Research Nurse RN, you need a solid background in nursing practice, clinical research protocols, and regulatory compliance, generally supported by a nursing degree, RN license, and research experience. Familiarity with clinical trial management systems, electronic data capture (EDC) tools, and certifications like CCRC or CCRP is important. Attention to detail, strong organizational abilities, and effective communication skills help ensure accurate data collection and collaboration with research teams and participants. These competencies are critical for maintaining research integrity, patient safety, and successful study outcomes.

What is the difference between Clinical Research Nurse Rn vs Clinical Research Coordinator?

AspectClinical Research Nurse RnClinical Research Coordinator
CredentialsRN license, nursing certificationBachelor's degree, research training
Work EnvironmentHospitals, clinics, research sitesResearch sites, hospitals, clinics
Employer & IndustryPharmaceutical companies, hospitals, research institutionsResearch organizations, hospitals, academic institutions
Primary FocusPatient care, safety, and data collectionStudy coordination, protocol management

While both roles are integral to clinical research, the Clinical Research Nurse Rn primarily focuses on patient care and safety within research studies, utilizing nursing skills and certifications. The Clinical Research Coordinator manages study logistics, protocol adherence, and data collection. Both roles often collaborate but differ in daily responsibilities and required credentials.

What is a Clinical Research Nurse RN?

A Clinical Research Nurse RN is a registered nurse who specializes in conducting and managing clinical trials and research studies involving human participants. Their responsibilities include recruiting participants, administering study treatments, collecting data, ensuring compliance with research protocols, and maintaining patient safety. They work closely with physicians, researchers, and regulatory bodies to ensure the integrity and ethical conduct of the research. Clinical Research Nurses play a vital role in advancing medical knowledge and improving patient care through evidence-based research.

What are some common challenges Clinical Research Nurses (RNs) face when balancing patient care with study protocol requirements?

Clinical Research Nurses often navigate the challenge of delivering high-quality patient care while strictly adhering to complex clinical trial protocols. Balancing these responsibilities can be demanding, as patient needs must be met without compromising data integrity or regulatory compliance. Effective communication with multidisciplinary teams and meticulous attention to detail are crucial to ensure both patient safety and study accuracy. Many find that developing strong organizational skills and maintaining open lines of communication with investigators, coordinators, and patients helps manage these competing priorities successfully.
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Clinical Research Nurse Rn jobs near you
Clinical Research Nurse

Clinical Research Nurse

Alcanza Clinical Research

Decatur, GA

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 15 days ago

Job description

Description
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Clinical Research Nurse works to ensure the execution of assigned studies, and performs clinical procedures, such as venipunctures, injections, prep or mixing of investigational study drugs and infusions, under the scope of the study protocol and in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.

Key Responsibilities
Essential Job Duties: In collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:
  • Under the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes & procedures, and in compliance with FDA, GCP, ICH regulations and guidelines: 
    • Screening of patients for study enrollment; 
    • Patient consents; 
    • Patient follow-up visits; 
    • Documenting in source clinic charts; 
    • Entering data in EDC and answers queries; 
    • Obtaining vital signs and ECGs; 
    • May perform basic lab procedures per protocol, such as:  blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; 
    • Performing procedures commensurate with licensure including vitals, ECGs/EKGs, venipunctures, injections, infusions, mixing drug and/or dispense investigational product; etc. 
    • Requesting and tracking medical record requests; 
    • Updating and maintaining logs, chart filings; 
    • Maintaining & ordering study specific supplies; 
    • Scheduling subjects for study visits and conducts appointment reminders; 
    • Building/updating source as needed; 
    • Conducting monitoring visits and resolves issues as needed in a timely manner; 
    • Ensuring study related reports and patient results are reviewed by investigator in a timely manner; 
o    Filing SAE/Deviation reports to Sponsor and IRB as needed;
o    Documenting and reporting adverse events;
o    Reporting non-compliance to appropriate staff in timely manner;
o    Maintaining positive and effective communication with clients and team members;
o    Always practicing ALCOAC principles with all documentation;
 
  • Be thoroughly familiar with the protocol, case report form, informed consent, source documentation, patient diary (when applicable), and study medication(s) for the assigned research study;
  • Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;
  • Prepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;
  • May set up, train and maintain all technology needed for studies.
  • May assist with study recruitment, patient enrollment, and tracking as needed;
  • Maintaining confidentiality of patients, customers and company information, and;
  • Performing all other duties as requested or assigned. 

Skills, Knowledge and Expertise
Minimum Qualifications:  A Bachelor’s degree in Nursing (BSN) AND a minimum of 1 year of clinical experience, OR an equivalent combination of education and experience, is required.  An active, unrestricted RN license, in state of work location, is required.  BLS certification required.  Bi-lingual (English / Spanish) proficiency is a plus. 

 Required Skills: 

  • Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);
  • Proficiency with performing clinical procedures such as injections, vitals, EKGs, phlebotomy, infusions, etc. is required.  
  • Strong organizational skills and attention to detail.
  • Well-developed written and verbal communication skills. 
  • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
  • Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
  • Must be professional, respectful of others, self-motivated, and have a strong work ethic.
  • Must possess a high degree of integrity and dependability.
  • Ability to work under minimal supervision, identify problems and implement solutions.
  • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

Benefits
  • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire. 
  • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.