Rn Clinical Research - Austin, United States - Austin Heart

Austin Heart

Verified Company

Austin, United States

3 weeks ago

Posted by:

Mark Lane

beBee recruiter

Description

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, longterm 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 employeeonly coverage to fulltime and parttime 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 noncompliance 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