Registered Nurse Research
Company: Beaumont Health
Location: Royal Oak
Posted on: June 16, 2022
|
|
Job Description:
Research RNFull time/Day shiftSummary: -The Clinical Research
Nurse will provide clinical support in the Cancer clinical trials
office.The Clinical Research Nurse role is the specialized practice
of professional nursing focused on maintaining equilibrium between
care of the research participant and fidelity to the research
protocol. This specialty practice incorporates human subjects
protection, care coordination and continuity, contribution to
clinical science, clinical practice and study management throughout
a variety of professional roles (i.e., study coordinator,
regulatory, monitor), practice settings, and clinical specialties.
-Standard Requirements:A. - -Education / Training: -BSN required.
-B. - -Work Experience: -Prior medical/surgical clinical experience
required; 2 year minimum. -Current phlebotomy skills highly
preferred. MS Word, Excel, Outlook, and Epic (OneChart) experience
required. -C. - -Certification, Licensure, Registration: MI
Registered Nurse license. -National research certification (SoCRA
or ACRP) within three to five years of hire date required. -BLS
Healthcare Provider Certification required. Department specific
clinical certification and/or experience may be required. -D. -
-Other Qualifications: -Must demonstrate expert clinical skills,
show well-developed critical thinking skills, and integrate
knowledge of regulatory, ethical and scientific aspects of clinical
research into practice. -Knowledge of FDA Regulations and Good
Clinical Practices. Must be able to work autonomously. Excellent
verbal, written and organizational skills required.Preferred
Requirements: ---- - - -Clinical Research experience highly
preferred. -Essential Duties: -1. - - -The Clinical Research Nurse
ensures human subject protections via diligence in research
participant screening, recruitment, consenting, enrollment,
monitoring of treatment, and follow-up procedures, ongoing risk
assessment related to research interventions and protocol
activities. -2. - - -Ensures ongoing research informed consent,
addresses participant questions throughout study participation and
supports their goal for participating or terminating study
participation. -3. - - -Coordinates research activities to minimize
participant risk. -4. - - -Distributes study article (drugs,
devices), administers study drug, and maintains study article
accountability documentation.5. - - -Provides care coordination and
continuity, integrating research and clinical activities to meet
clinical needs of research participants, coordinates and completes
research protocol activities, communicates with referring providers
when necessary. -6. - - -Facilitates education of research teams
related to study requirements. -7. - - -Ensures plan of care for
research participant is safe and allows for effective collection of
clinical research data. -8. - - -Documents all study-related
procedures/events via electronic data capture systems, case report
forms, etc.9. - - -Communicates effectively with research
participants and their families, the research team, principal
investigators, external study sponsors, primary care providers
(e.g., clinical nurses, physicians, etc.), ancillary staff and the
IRB to ensure protocol adherence, participant safety and Regulatory
compliance.To perform this job successfully, an individual must be
able to perform each essential duty satisfactorily. -The
requirements listed below are representative of the knowledge,
skill and/or ability required. -Reasonable accommodations may be
made to enable individuals with disabilities to perform the
essential duties.ACKNOWLEDGEMENT OF EMPLOYMENT UNDER RESEARCH
GRANT
Keywords: Beaumont Health, Royal Oak , Registered Nurse Research, Healthcare , Royal Oak, Michigan
Click
here to apply!
|