Clinical Research RN

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

Work location: 8440 Walnut Hill Lane Ste 220; Dallas TX 75231
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

Heres What You Need

Associates Degree in nursing required
Bachelors 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 strongly 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 Sponsors 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 protocols 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 subjects 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

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