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Rn Clinical Research

4 months ago


Austin, United States Austin Heart Full time

**Introduction**:
Do you want to join an organization that invests in you as a(an) RN Clinical Research? At Austin Heart, you come first. HCA Healthcare has committed up to $300 million in programs to support our incredible team members over the course of three years.

**Benefits**:
Austin Heart, offers a total rewards package that supports the health, life, career and retirement of our colleagues. The available plans and programs include:

- Comprehensive medical coverage that covers many common services at no cost or for a low copay. Plans include prescription drug and behavioral health coverage as well as free telemedicine services and free AirMed medical transportation.
- Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more.
- Free counseling services and resources for emotional, physical and financial wellbeing
- 401(k) Plan with a 100% match on 3% to 9% of pay (based on years of service)
- Employee Stock Purchase Plan with 10% off HCA Healthcare stock
- Family support through fertility and family building benefits with Progyny and adoption assistance.
- Referral services for child, elder and pet care, home and auto repair, event planning and more
- Consumer discounts through Abenity and Consumer Discounts
- Retirement readiness, rollover assistance services and preferred banking partnerships
- Education assistance (tuition, student loan, certification support, dependent scholarships)
- Colleague recognition program
- Time Away From Work Program (paid time off, paid family leave, long
- and short-term disability coverage and leaves of absence)
- Employee Health Assistance Fund that offers free employee-only coverage to full-time and part-time colleagues based on income.

Learn more about Employee Benefits

**_ Note: Eligibility for benefits may vary by location._**

You contribute to our success. Every role has an impact on our patients’ lives and you have the opportunity to make a difference. We are looking for a dedicated RN Clinical Research like you to be a part of our team.

**Job Summary and Qualifications**:
**SUMMARY OF DUTIES**:
Responsible for assessing proposed study protocols and for the coordination and implementation of all nursing and administrative activities related to clinical trials. Performs within the parameters for which he or she is qualified by education, training, experience and licensure.

**DUTIES INCLUDE BUT NOT LIMITED TO**:

- Coordinates all research study activities with the Principal Investigator and has direct nursing care responsibilities.
- Coordinates and manages clinical studies according to OHRP and FDA regulations, as well as, ICH Good Clinical Practices and IRB requirements.
- Develops tactical study procedures
- Develops any necessary study documents not provided by sponsor or IRB
- Educates HCA staff regarding research and study protocols
- Screens and recruits patients based on protocol criteria
- Explains study protocols, procedures and treatments to patients and families
- Conducts the Informed Consent process in conjunction with study investigators
- May function as Primary Coordinator for research studies
- Responsible for all investigational drug accountability and dispensing
- Coordinates with Pharmacist if on Delegation Log
- Administers Investigational Drug as per protocol
- Serve as a resource for department members for medical interpretations of research process and protocol specifics
- Assess each proposed study protocol with critical analysis of potential implementation and patient care - Dedicate to creative/innovative growth of research in the division
- Acquire continuing education pertinent to research and applicable licensed profession
- Responsible for maintaining good clinical practice standards, addressing non-compliance issues, developing corrective action plans
- Execute medical orders within parameters of education, training and licensure
- Conduct study activities helping to ensure all safety parameters
- Investigational device accounting and dispensing
- Facilitate administrative review and approval of proposed studies
- Provide/coordinate the highest level of contact, counseling and support services
- Coordinate study activities and patient care with medical staff (cardiologist and PCP, etc.)
- Implement and adhere to study protocol
- Perform Phlebotomy and IV procedures
- Prepare laboratory specimens for analysis, monitoring tests and procedures, shipping frozen specimens
- Maintain patient records in EMR and appropriate hospital records
- Assess and report adverse study events, included to the IRB and any research sponsors
- Complete all paperwork affiliated with the study, including but not limited to the requirements of the facility, the IRB and the stu