Research RN 1
About The Position
As a Research Nurse 1, you'll assist principal investigators with clinical trials following guidelines. Gain knowledge on trial phases from start to finish. Learn all aspects of the position. You will learn to review new study protocols and materials from sponsors. You will screen patients for clinical trial eligibility according to HIPAA standards, which is a core part of your role. You'll help complete study activities by returning supplies, disposing unused stock, and addressing all queries thoroughly. Your responsibilities will also extend to assisting with the preparation of final reports for the Institutional Review Board. You'll develop skills to effectively use the Study Assistant Clinical Trials Management System, as per departmental requirements.
Requirements
- Active RN licensure with strong clinical assessment skills
- Strong attention to detail and documentation skills
- Ability to identify and escalate patient safety concerns promptly
- Excellent verbal and written communication skills
- Ability to build rapport with research participants
- Professional and courteous interaction with physicians, sponsors, CROs, and colleagues
- Strong collaboration skills within a multidisciplinary team
- Strong time management and prioritization abilities
- Ability to manage multiple studies and competing deadlines
- Excellent organizational and follow-up skills
- Ability to maintain accurate and complete research records
- Patient-focused and compassionate
- Self-motivated and proactive
- Adaptable in a fast-paced environment
- Problem-solving mindset
- Commitment to quality, compliance, and continuous learning
- Associate's degree.
- Registered Nurse (RN) License.
- BLS certification within 30 days.
Nice To Haves
- Bachelor's degree in nursing
- Clinical research experience
- Epic Experience
- Spanish speaking
- Cardiovascular background
Responsibilities
- Collaborating with departments on research.
- Working under a research head.
- Interacting with investigators and managers.
- Provide education for healthcare professionals.
- Coordinate with Pharmacy for projects.
- Review new study protocols and materials from sponsors.
- Screen patients for clinical trial eligibility according to HIPAA standards.
- Complete study activities by returning supplies, disposing unused stock, and addressing all queries thoroughly.
- Assist with the preparation of final reports for the Institutional Review Board.
- Develop skills to effectively use the Study Assistant Clinical Trials Management System, as per departmental requirements.
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What This Job Offers
Career Level
Entry Level
Education Level
Associate degree
