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Part Time Clinical Trial Rn Jobs (NOW HIRING)

Denali Health

Clinical Research Nurse

Atlanta, GA · On-site

This position offers flexible scheduling while providing critical support to our clinical trial ... Current Registered Nurse (RN) license in the State of Georgia * Minimum 1-2 years of clinical ...

Home Careolina

Registered Nurse

Cornelius, NC · On-site

$35 - $40/hr

Registered Nurse (RN) - Part-Time Clinical Support & Care Management Home Careolina Lake Norman Region Home Careolina is seeking an experienced Registered Nurse (RN) to join our growing team in a ...

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Part Time Clinical Trial Rn information

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How much do part time clinical trial rn jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for part time clinical trial rn in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

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

AspectPart Time Clinical Trial RnPart Time Research Nurse
CredentialsRegistered Nurse (RN) license, clinical trial certificationsRegistered Nurse (RN) license, research-specific training
Work EnvironmentClinical trial sites, hospitals, research facilitiesResearch settings, hospitals, clinics
Employer & IndustryPharmaceutical companies, CROs, research institutionsAcademic institutions, hospitals, research organizations
Job FocusManaging clinical trial procedures, patient care in trialsSupporting research studies, data collection, patient monitoring

Both roles require RN licensure and involve working in research environments. The main difference lies in their focus: Part Time Clinical Trial Rns primarily manage clinical trial procedures and patient care within trials, while Part Time Research Nurses support research activities, data collection, and study coordination. Understanding these distinctions helps candidates choose the role that best fits their skills and career goals.

What is a Part Time Clinical Trial RN?

A Part Time Clinical Trial RN (Registered Nurse) is a nurse who works on a part-time basis to support clinical research studies. They are responsible for administering study medications, monitoring patient health, collecting data, and ensuring that trials adhere to regulatory and ethical standards. This role often involves working closely with physicians, research coordinators, and patients to facilitate the safe and effective conduct of clinical trials. Part Time Clinical Trial RNs typically have flexible schedules and may work in hospitals, research centers, or outpatient clinics.

How does a part-time Clinical Trial RN typically balance patient care with research documentation responsibilities?

As a part-time Clinical Trial RN, you will often need to efficiently manage your time between direct patient care—such as administering investigational medications and monitoring for side effects—and completing detailed research documentation required for regulatory compliance. Many RNs find that staying organized and proactively communicating with the research team helps manage these dual responsibilities. You'll likely work closely with principal investigators, coordinators, and other healthcare professionals to ensure both patient safety and accurate data collection, often attending regular team meetings to discuss trial progress and any patient concerns.

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

To thrive as a Part Time Clinical Trial RN, you need a solid background in nursing practice, clinical research protocols, and a valid RN license, often with experience in clinical trials or research settings. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and regulatory documentation is typically required. Attention to detail, strong organizational skills, and the ability to communicate effectively with both patients and research teams are standout soft skills. These competencies ensure accurate data collection, patient safety, and compliance with study protocols, which are critical for successful clinical research outcomes.
What cities are hiring for Part Time Clinical Trial Rn jobs? Cities with the most Part Time Clinical Trial Rn job openings:
What are the most commonly searched types of Clinical Trial Rn jobs? The most popular types of Clinical Trial Rn jobs are:
What states have the most Part Time Clinical Trial Rn jobs? States with the most job openings for Part Time Clinical Trial Rn jobs include:
Part Time Clinical Trial Rn jobs near you
Part Time Clinical Research Coordinator

Part Time Clinical Research Coordinator

SerenaGroup

Monroeville, PA • On-site

$53K - $58K/yr

Part-time

Re-posted 2 days ago

Job description

Job Type
Part-time
Description
The Clinical Research Coordinator (CRC) at SerenaGroup plays a critical role in the execution of clinical trials focused on advanced wound care and hyperbaric medicine. This position is responsible for coordinating all aspects of clinical research studies, ensuring compliance with regulatory guidelines, and supporting high-quality patient care and data integrity throughout the study lifecycle.
The CRC will work collaboratively with Principal Investigators, Clinical Trial Leads, sponsors, and cross-functional teams to ensure studies are conducted efficiently, ethically, and in alignment with SerenaGroup's commitment to evidence-based care and improved patient outcomes.
Key Responsibilities
Study Coordination & Execution
  • Coordinate and manage day-to-day clinical trial activities from study start-up through close-out
  • Schedule and conduct study visits in accordance with protocol requirements
  • Ensure proper informed consent is obtained and documented for all study participants
  • Maintain accurate and up-to-date study documentation, including regulatory binders and source documents

Patient Care & Engagement
  • Identify, recruit, and screen eligible patients for clinical trials
  • Educate patients on study protocols, procedures, and expectations
  • Monitor patient safety and report adverse events in accordance with regulatory requirements

Data Management & Compliance
  • Accurately collect, record, and enter study data into electronic data capture (EDC) systems
  • Perform source data verification (SDV) and ensure data integrity and completeness
  • Ensure compliance with FDA regulations, ICH-GCP guidelines, and SerenaGroup SOPs

Collaboration & Communication
  • Serve as a liaison between investigators, sponsors, CROs, and internal teams
  • Support monitoring visits, audits, and regulatory inspections
  • Communicate effectively with cross-functional teams to ensure study milestones are met

Qualifications
Education & Experience
  • Bachelor's degree in life sciences, healthcare, or related field preferred
  • 1-3 years of experience in clinical research or healthcare setting (wound care experience a plus)
  • Experience working with clinical trial protocols and regulatory requirements preferred

Skills & Competencies
  • Strong organizational and time management skills
  • High attention to detail and accuracy in documentation
  • Excellent interpersonal and communication skills
  • Ability to manage multiple studies and priorities in a fast-paced environment
  • Proficiency in EDC systems and Microsoft Office Suite

Preferred Qualifications
  • Certification as a Clinical Research Coordinator (e.g., ACRP or SOCRA)
  • Experience in wound care, hyperbaric medicine, or related therapeutic areas
  • Familiarity with clinical trial start-up and regulatory submissions

Salary Description
$53,000-$58,000

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