Registered Nurse — Exciting PRN Clinical Research Role
Revival Research Institute, LLC
Behavioral Health Market Context
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Qualifications
- •An interest in clinical research is a strong plus and provides a solid foundation for this entry-level opportunity with room to advance
- •Bachelor’s degree in a health-related field with 1–2 years of relevant clinical experience, OR
- •Master’s degree in a medical-related field with no prior research experience
- •Candidates with additional experience may be considered for higher-level roles
- •Additional Skills & Certifications
- •BLS certification required
- •Strong computer and database skills, including Microsoft Word, Excel, and Outlook
- •Excellent verbal and written communication skills
- •Strong organizational abilities and attention to detail
- •Ability to work independently, meet deadlines, and maintain confidentiality
- •Ability to work collaboratively with physicians, PRN nurses, technicians, administrative staff, and ancillary personnel
- •Knowledge of FDA regulations and Good Clinical Practice guidelines
- •9 more items(s)
Responsibilities
- •Our PRN Nurses work closely with our Clinical Research Coordinators and support Investigators and clinical staff with a variety of study-related responsibilities, including but not limited to:
- •Participating in participant screening, recruitment, and enrollment
- •Consenting participants and conducting research visits for data collection (no-risk or minimal-risk trials, with oversight)
- •Collecting, processing, and shipping research specimens (where applicable)
- •Documenting study information in case report forms or electronic data capture systems; resolving data queries; supporting monitoring visits
- •Obtaining, reviewing, and maintaining accurate source documentation
- •Maintaining organization of all study documentation and correspondence
- •Implementing quality control and quality assurance procedures
- •Communicating with sponsors, the research team, and the Institutional Review Board
- •Assisting with basic regulatory document preparation (amendments, adverse event reporting, protocol deviation reporting)
- •Maintaining professional and technical knowledge related to clinical trials
- •Communicating effectively with research participants and families while protecting confidentiality
- •Additional Study-Related Responsibilities (Unblinded Duties)
- •Receiving and registering investigational product (IP) in the IWRS
- •Dispensing and preparing weekly medication for randomized subjects per protocol and pharmacy guidelines
- •Performing full IP accountability
- •Completing subject-level and master IP logs
- •Participating in unblinded monitoring visits
- •Completing all assigned unblinded and general study-related training tasks
- •Performing additional duties as assigned by the unblinded team
- •17 more items(s)
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