Clinical Research Nurse
Denali Health · Atlanta, Georgia, United States · Posted Jul 3, 2026
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About Denali Health:
Denali Health is an Independent Research Organization (IRO) dedicated to accelerating the development of innovative therapies to market. We conduct Phase I-IV clinical trials across multiple therapeutic areas, including neurology, psychiatry, wound care, and other specialty areas. Our commitment to excellence in clinical research operations ensures the highest standards of patient care and scientific integrity.
Position Summary:
We are seeking an experienced Clinical Research Nurse to join our Atlanta team on a PRN basis. This position offers flexible scheduling while providing critical support to our clinical trial operations. The ideal candidate will have a strong foundation in clinical research nursing, excellent patient care skills, and the ability to work independently in a dynamic research environment.
Key Responsibilities:
Conduct patient screening, enrollment, and study visits according to protocol requirements
Perform clinical assessments, vital signs, phlebotomy, ECGs, and other study-related procedures
Administer investigational products and medications per protocol specifications
Ensure accurate and timely documentation in source documents and electronic data capture systems
Monitor patient safety and report adverse events in compliance with regulatory requirements
Educate patients and families about study procedures, informed consent, and expectations
Maintain regulatory compliance with FDA, ICH-GCP, and institutional guidelines
Coordinate with Principal Investigators, study coordinators, sponsors, and CROs
Assist with patient recruitment and retention activities
Maintain study supplies, equipment, and laboratory specimens
Required Qualifications:
Current Registered Nurse (RN) license in the State of Georgia
Minimum 1-2 years of clinical nursing experience
Valid BLS certification
Strong clinical assessment and procedural skills
Excellent communication and interpersonal abilities
Attention to detail and strong organizational skills
Ability to work independently and as part of a collaborative team
Proficiency with electronic medical records and data capture systems
Flexibility to work as needed based on study demands
Preferred Qualifications:
Previous clinical research experience
CCRP (Certified Clinical Research Professional) or ACRP certification
Experience with Phase I-IV clinical trials
Familiarity with ICH-GCP guidelines and FDA regulations
Phlebotomy certification
Experience in neurology, psychiatry, wound care, or specialty therapeutic areas
Bilingual capabilities (Spanish or other languages)
What We Offer:
Competitive PRN hourly rate
Flexible scheduling to accommodate your availability
Opportunity to work on cutting-edge clinical research
Exposure to diverse therapeutic areas and study phases
Professional development in clinical research
Collaborative and supportive work environment
Potential for increased hours based on the study pipeline
Physical Requirements:
Ability to stand and walk for extended periods
Manual dexterity for performing clinical procedures
Ability to lift up to 25 pounds
Visual acuity for detailed documentation and patient assessment
Note: This is a part-time position that requires working one week per month on-site according to the following schedule:
Tuesday - Friday: Night shift
Saturday - Sunday – Monday: Full-day shift (9:00 AM – 5:00 PM)
Please ensure you are available to commit to this schedule before applying.