Registered Nurse (RN) PRN

Revival Research Institute, LLC•Denton, TX

About The Position

Unique Opportunity to Make an Impact in the Healthcare Industry Revival Research Institute, LLC was established in 2015 and is headquartered in the Metro Detroit region. Since then, we have continued to grow—now operating across Michigan, Texas, Illinois, North Carolina, and Georgia. We have been nationally recognized for our diligence and commitment to delivering the highest quality data in our clinical research trials. As Revival Research Institute continues to expand, we are seeking motivated, detail-oriented professionals who want to develop their careers and learn alongside a rapidly growing organization. We are currently seeking a Registered Nurse (RN) PRN with a minimum of one year of clinical experience. An interest in clinical research is a strong plus and provides a solid foundation for this entry-level opportunity with room to advance. However, prior research experience is not required. Our ideal candidate is organized, attentive to detail, eager to learn, and excited to grow with us as our company expands into new therapeutic areas. At Revival, we foster a culture of respect, inclusiveness, and collaboration. 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 IMPROVE THE FUTURE AS OUR NEXT CLINICAL RESEARCH COORDINATOR!

Requirements

minimum of one year of clinical experience
organized
attentive to detail
eager to learn
excited to grow with us as our company expands into new therapeutic areas
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

Nice To Haves

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
Phlebotomy skills preferred
National research certification (CRA or ACRP) preferred
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

Responsibilities

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
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