Clinical Research Nurse

BayCare Health System

Tampa, FLFull-timeSeen todaySeen in employer's feed today

Tampa, FLFull-timeNo compensation foundSeen todaySeen in employer's feed today

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At a glance

Compensation

No compensation found

Location

Tampa, FL

Schedule

Full-time

Work Authorization

Not specified

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Requirements

Credentials this posting asks for.

RNAssociate's degree

Job overview

BayCare Health System seeks a Clinical Research Nurse to coordinate and implement research studies, ensure protocol adherence, schedule patient visits, manage regulatory documents, obtain consent, and conduct clinical follow‑up, while reporting adverse events and maintaining investigational product accountability within a collaborative, forward‑thinking environment.

Skills & qualifications

RequiredNice to have

Skills

Good Clinical PracticeIRB ComplianceHIPAA AuthorizationPatient SchedulingStudy RecruitmentRegulatory DocumentationInformed ConsentElectronic Data CaptureCase Report FormAdverse Event ReportingInvestigational Product AccountabilityIndependent Judgment

Qualifications

RNCCRCAssociates in NursingDiploma in NursingBachelors in Nursing2 Years Healthcare or Management ExperienceClinical Research Experience

Benefits

Medical Insurance

Dental Insurance

Vision Insurance

Paid Time Off

Tuition Assistance

401(k) Match

Full job description

Join the team that is revolutionizing health care – BayCare Health System

Our network consists of 16 community-based hospitals, a long-term acute care facility, home health services, outpatient centers and thousands of physicians. With the support of more than 30,000 team members, we promote a forward-thinking philosophy that’s built on a foundation of trust, dignity, respect, responsibility, and clinical excellence.

Title: Clinical Research Nurse

Facility: St. Joseph's Hospital

Responsibilities:

Coordinates and implements research studies for assigned services under the direction of the Principal investigator in accordance with the standards of good clinical practice, federal and state regulations and institutional review board (IRB) requirements
Ensures adherence to the study protocol and schedule of events
Patient visit scheduling for protocol related procedures
Screening, study recruitment, preparation of IRB reports
Establishment and maintenance of regulatory documents
Performing the process of informed consent and HIPPA authorization
Clinical follow-up of study subjects
Creation and completion of source worksheets,
Collecting source data for electronic data capture (EDC) systems or Case Report Form (CRF) completion
Assesses patients for trial-related and non-trial related symptoms
Reporting of adverse events, serious adverse events, and dispensing / accountability of investigational product
Must work independently and use sound judgment while performing job duties
Performs duties as assigned under the scope of related certification or licensure