Clinical Research RN - Full time

Texas Health Resources -
Fort Worth, TX

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Job Details

Full-time

Benefits

Paid parental leave
Health insurance
Dental insurance
401(k)
Tuition reimbursement
Paid time off
Parental leave
Loan forgiveness

Qualifications

RN License
Associate's degree
Associate Degree in Nursing

Full Job Description

Clinical Research RN
Bring your passion to Texas Health so we are Better + Together

Work location: Texas Health Fort Worth: 1300 W Terrell Ave, ste K250; Fort Worth, Texas 76104
Work hours: Monday – Friday from 8am – 5pm

Department highlights:

Strong team with strong, collaborative relationships
Works closely with the Cardiovascular Structural Heart team
Opportunity to innovate healthcare

Here’s What You Need

Associate’s Degree in nursing required
Bachelor’s degree in nursing preferred
6 months ICU/CCU/ ER experience or equivalent required or
2 years conducting clinical research (drug, devices, etc) required
Clinical Research experience preferred
Research training via CITI (Human subject Protection and Good Clinical Practice) preferred
Epic EMR, Realtime CTMS and SharePoint experience preferred
Dangerous Shipping Goods/Materials Certificate preferred
RN upon hire required
ACLS upon hire preferred
CPR within 30 days of hire and maintained every 2 years

What You Will Do

Conduct clinical studies according to FDA, CFR and ICH regulations and guidelines: from pre-study to startup to closeout. Including: Study Startup: coordination and facilitation of all departments and various organizations to successfully startup a study from feasibility to first
Be knowledgeable of the Sponsor’s protocol so that all study activities are completed correctly and completely. Train other site personnel, and medical staff, on the specifics of implementing assigned protocols; including the regulations and expectations of monitors. Educate participants, families and caregivers regarding protocol requirements and relationship to disease process. Communicate and meet with the Sponsors, IRBs, Physicians, regulatory bodies, etc. regarding essential study activities as

necessary, such as the conduct of the study and review study data. Promote and represent the CRD in a positive manner

Develop and implement recruitment strategies for studies; which include screening potential study subjects according to the protocol’s inclusion and exclusion criteria. Be available to register participants after hours (on call 24 hours a day and on weekends).
Schedule study subjects’ visits and during the study subject’s visit perform defined activities of the study completely and accurately. Complete the CRFs for the study accurately, completely, and in a timely fashion. Maintain adequate and accurate case histories for each study subject and record all observations in the source document during the study. Complete the adverse events source documentation for the sponsor and IRB for review by the Investigator. Including: Design and maintain organizational tools to conduct studies accurately and in compliance with GCP and ICH guidelines.
Ensure the safety and welfare of the study subjects. Obtain proper written information consent from each study subject prior to participate in the study
Maintain all information in original records and certified copies of original records of clinical findings, observations, or other activities in a clinical trial necessary for the reconstruction and evaluation of the trial. Source data are contained in source documents (original records or certified copies) (ICH 1.51). Unless original copies are required to be kept by the Sponsor (i.e. EKG tracings, patient diaries, questionnaires, etc), then a note to file is placed in the study regulatory binder. Follows electronic source guidelines and certification and destruction of hard copies, when applicable. Including: Assign study subject numbers and maintain accurate and complete records of the receipt, administration, and return of all clinical supplies (including study drug). Assist in maintaining all required documentation in the study regulatory documentation file. Including processing and completing all IRB documentation. Including but not limited to: initial application, Informed Consent, modifications, amendments, Serious Adverse Events, advertisement, etc.
Obtain and maintain certification through appropriate accrediting bodies: (RN, and BLS) As well as certification and training required for studies: GCP, HSP, etc

Additional perks of being a Texas Health Clinical Research RN

Benefits include 401k, PTO, medical, dental, Paid Parental Leave, flex spending, tuition reimbursement, student Loan forgiveness as well as several other benefits.
Delivery of high quality of patient care through nursing education, nursing research and innovations in nursing practice.
Strong Unit Based Council (UBC).
A supportive, team environment with outstanding opportunities for growth.
Learn more about our culture, benefits, and recent awards.
Do you still have questions or concerns? Feel free to email your questions to [email protected].

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