Registered Nurse Clinical Research Coordinator

Ascension•Pensacola, FL

22h•Onsite

About The Position

This role involves leading the execution of clinical study protocols, providing specialized nursing care, administering test interventions, and ensuring continuity of patient care through collaboration with multidisciplinary providers. The position also includes managing participant selection, informed consent, protocol education, clinical testing, and ongoing safety monitoring to support trial retention and participant well-being. Additionally, the role requires preparing, submitting, and tracking internal and external regulatory documentation (e.g., IRB, FDA) across all trial phases, while actively driving quality assurance/improvement initiatives and maintaining applicable standards of care. Accurate, compliant clinical care and study data recording into appropriate databases is essential, along with systematically communicating trial findings, adverse events, and progress updates to the broader research team.

Requirements

Licensed Registered Nurse credentialed from the Florida Board of Nursing obtained prior to hire date or job transfer date required.
Licensed as a Registered Nurse in Florida required.
Credentialed from State Board of Nursing or current home state license for multi-state license recognition "Compact State" obtained prior to hire date or job transfer date required.
Diploma from an accredited school/college of nursing OR Required professional licensure at time of hire.

Nice To Haves

Prior cardiology or neurology RN experience

Responsibilities

Lead study execution according to specific clinical protocols, providing specialized nursing care, administering test interventions, and ensuring continuity of care through collaboration with multidisciplinary providers.
Manage participant selection, informed consent, protocol education, clinical testing, and ongoing safety monitoring to support trial retention and participant well-being.
Prepare, submit, and track internal and external regulatory documentation (e.g., IRB, FDA) across all trial phases, while actively driving quality assurance/improvement initiatives and maintaining applicable standards of care.
Record accurate, compliant clinical care and study data into appropriate databases, systematically communicating trial findings, adverse events, and progress updates to the broader research team.