Director, Clinical Research 916733
Company Name:
Vidant Health
About Vidant Medical Center
Vidant Medical Center is a fully accredited, 900
bed regional referral facility encompassing a Level-1 Trauma Center and extensive inpatient and outpatient services including intensive and intermediate care, pediatrics, bariatrics, obstetrics and gynecology, surgery, pain management and psychiatry. Vidant Medical Center recently received Magnet designation from the American Nurses Credentialing Center (ANCC). Magnet recognizes health care organizations for quality patient care, nursing excellence and professional practice.
Responsibilities
The Director for Clinical Research provides administrative oversight for the Clinical Research program/department at Vidant Medical Center. This position provides assurance for the protection of human subjects in Clinical Research and serves as a required institutional liaison to the UMCIRB. The Director for Clinical Research is responsible for dissemination of knowledge to improve clinical practice and patient outcomes across Vidant Medical Center. This position provides a leadership role for planning, developing, implementing and evaluating a comprehensive Nursing Clinical Research Program across clinical, educational and administrative practice. The Director for Clinical Research monitors and mentors Clinical Research activities conducted at Vidant Medical Center and serves as a liaison with departments and outside agencies on Clinical Research activities being conducted at Vidant Medical Center.
Administrative oversight of Clinical Research Program based. Facilitate and mentor nursing personnel to develop, conduct and disseminate Clinical Research studies. Foster the development of a practice environment conducive to the conduct and utilization of Clinical Research.
Develop resources that foster staff involvement and use of the Clinical Research process. Integrate Clinical Research and evidence based activities with quality and patient safety.
Manage fiscal and personal resources in Clinical Research Office.
Design and conducts Clinical Research studies.
Consult with staff, students, clinical and administrative groups, physicians and residents on Clinical Research projects and process.
Serve as Vidant Medical Center Human Protection Director for Office of Human Clinical Research Protection.
Review coordinate, track and monitor Clinical Research proposal/activities to be conducted at Vidant Medical Center involving Vidant Medical Center employees, Clinical Researchers conducting studies at Vidant Medical Center and patients of Vidant Medical Center.
Attend bi-weekly UMCIRB meetings and Institutional Review Meetings.
Liaison with VP, Directors and Managers for approval of Clinical Research studies within Vidant Medical Center service lines.
Meet monthly with UMCIRB representatives, ECU Clinical Research Compliance, BSOM Clinical Research compliance,
Vidant Medical Center Compliance, BSOM Clinical Trials Manager to address Clinical Research compliance issues.
Serve as a Clinical Research consultant to agencies outside of Vidant Medical Center i.e.: Vidant Health Corporate Hospitals, Human Protection Directors.
Facilitate Clinical Research within Vidant Medical Center and in the professional community.
Promote collaborative Clinical Research initiatives among nursing personnel, College of Nursing, and other health care agencies.
Collaborate with Vidant Medical Center Finance on clinical trial billing, BSOM Clinical Trial Office, HIMS, Pharmacy, Material Services, Laboratory, and Radiology on review of Clinical Research initiatives and compliance matters.
Work collaboratively with Health Sciences Library, Biostaticians, and other consultants on Clinical Research initiatives.
Serve on relevant nursing and Vidant Medical Center committees to develop and advance strategies and methods for integrating critical thinking and scientific rigor into practice, education, and management.
Collaborates in identification, measurement and evaluation of patient/family outcomes, especially those sensitive to nursing care.
Promote an environment conducive to Clinical Research process and utilization.
Facilitate and serves as a resource in preparation of abstracts, manuscripts, paper/poster presentations, grant initiatives.
Serve as a role model, mentor and educator for Vidant Medical Center staff at all levels with Clinical Research and evidence based practice.
Engage nursing staff, advanced practice nurses and managers in improving patient care outcomes and professional practice through involvement in Clinical Research initiatives.
Collaborate with nursing leaders and patient care service educators to provide Clinical Research in-service and continuing education program.
Demonstrates on-going professional career self-development.
Participates in Clinical Research educational programs and conferences.
Active member in professional organizations relevant to nursing Clinical Research and leadership (Southern Nursing
Clinical Research Society, CANS, AONE, NCONL, Sigma Theta Tau, ANA, NCNA, Phi Kappa Phi). Maintain active adjunct faculty status with East Carolina University.
Participate on local, state and national committees and task forces related to Clinical Research.
Minimum Requirements
Ph.D. or equivalent: Major: Nursing
5 years or greater, Previous experience with Clinical Research in clinical setting. Experience in qualitative and quantitative and qualitative methods necessary to evaluate program outcomes.
Human Protection Training
Registered Nurse Licensed in North Carolina
Apply Here: http://tinyurl.com/k4g8xphEstimated Salary: $20 to $28 per hour based on qualifications.
Vidant Health
About Vidant Medical Center
Vidant Medical Center is a fully accredited, 900
bed regional referral facility encompassing a Level-1 Trauma Center and extensive inpatient and outpatient services including intensive and intermediate care, pediatrics, bariatrics, obstetrics and gynecology, surgery, pain management and psychiatry. Vidant Medical Center recently received Magnet designation from the American Nurses Credentialing Center (ANCC). Magnet recognizes health care organizations for quality patient care, nursing excellence and professional practice.
Responsibilities
The Director for Clinical Research provides administrative oversight for the Clinical Research program/department at Vidant Medical Center. This position provides assurance for the protection of human subjects in Clinical Research and serves as a required institutional liaison to the UMCIRB. The Director for Clinical Research is responsible for dissemination of knowledge to improve clinical practice and patient outcomes across Vidant Medical Center. This position provides a leadership role for planning, developing, implementing and evaluating a comprehensive Nursing Clinical Research Program across clinical, educational and administrative practice. The Director for Clinical Research monitors and mentors Clinical Research activities conducted at Vidant Medical Center and serves as a liaison with departments and outside agencies on Clinical Research activities being conducted at Vidant Medical Center.
Administrative oversight of Clinical Research Program based. Facilitate and mentor nursing personnel to develop, conduct and disseminate Clinical Research studies. Foster the development of a practice environment conducive to the conduct and utilization of Clinical Research.
Develop resources that foster staff involvement and use of the Clinical Research process. Integrate Clinical Research and evidence based activities with quality and patient safety.
Manage fiscal and personal resources in Clinical Research Office.
Design and conducts Clinical Research studies.
Consult with staff, students, clinical and administrative groups, physicians and residents on Clinical Research projects and process.
Serve as Vidant Medical Center Human Protection Director for Office of Human Clinical Research Protection.
Review coordinate, track and monitor Clinical Research proposal/activities to be conducted at Vidant Medical Center involving Vidant Medical Center employees, Clinical Researchers conducting studies at Vidant Medical Center and patients of Vidant Medical Center.
Attend bi-weekly UMCIRB meetings and Institutional Review Meetings.
Liaison with VP, Directors and Managers for approval of Clinical Research studies within Vidant Medical Center service lines.
Meet monthly with UMCIRB representatives, ECU Clinical Research Compliance, BSOM Clinical Research compliance,
Vidant Medical Center Compliance, BSOM Clinical Trials Manager to address Clinical Research compliance issues.
Serve as a Clinical Research consultant to agencies outside of Vidant Medical Center i.e.: Vidant Health Corporate Hospitals, Human Protection Directors.
Facilitate Clinical Research within Vidant Medical Center and in the professional community.
Promote collaborative Clinical Research initiatives among nursing personnel, College of Nursing, and other health care agencies.
Collaborate with Vidant Medical Center Finance on clinical trial billing, BSOM Clinical Trial Office, HIMS, Pharmacy, Material Services, Laboratory, and Radiology on review of Clinical Research initiatives and compliance matters.
Work collaboratively with Health Sciences Library, Biostaticians, and other consultants on Clinical Research initiatives.
Serve on relevant nursing and Vidant Medical Center committees to develop and advance strategies and methods for integrating critical thinking and scientific rigor into practice, education, and management.
Collaborates in identification, measurement and evaluation of patient/family outcomes, especially those sensitive to nursing care.
Promote an environment conducive to Clinical Research process and utilization.
Facilitate and serves as a resource in preparation of abstracts, manuscripts, paper/poster presentations, grant initiatives.
Serve as a role model, mentor and educator for Vidant Medical Center staff at all levels with Clinical Research and evidence based practice.
Engage nursing staff, advanced practice nurses and managers in improving patient care outcomes and professional practice through involvement in Clinical Research initiatives.
Collaborate with nursing leaders and patient care service educators to provide Clinical Research in-service and continuing education program.
Demonstrates on-going professional career self-development.
Participates in Clinical Research educational programs and conferences.
Active member in professional organizations relevant to nursing Clinical Research and leadership (Southern Nursing
Clinical Research Society, CANS, AONE, NCONL, Sigma Theta Tau, ANA, NCNA, Phi Kappa Phi). Maintain active adjunct faculty status with East Carolina University.
Participate on local, state and national committees and task forces related to Clinical Research.
Minimum Requirements
Ph.D. or equivalent: Major: Nursing
5 years or greater, Previous experience with Clinical Research in clinical setting. Experience in qualitative and quantitative and qualitative methods necessary to evaluate program outcomes.
Human Protection Training
Registered Nurse Licensed in North Carolina
Apply Here: http://tinyurl.com/k4g8xphEstimated Salary: $20 to $28 per hour based on qualifications.
|
|
 | |
