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Valley Health System

Clinical Trials/ Research Super

Valley Health System, Ridgewood, New Jersey, us, 07450


Clinical Trials/ Research SuperPOSITION SUMMARY:

The Supervisor, Clinical Trials and Research Unit (S-CRTU), position is responsible for the administrative leadership, daily operations and clinical conduct of assigned clinical trials and research unit(s) of The Valley Hospital (TVH), i.e., cardiology, oncology, neurology etc. This position is responsible for oversight of all clinical research activities and participates as a main coordinator on studies. The position is responsible for oversight of all research personnel in a manner that effectively maximizes efficiency, quality and compliance with clinical research standards, patient safety, and physician satisfaction. Effectively manage staff and conduct performance assessments. Consistently support compliance and TVHs Code of Conduct and S.E.R.V.E. values by maintaining the privacy and confidentiality of information, acting with ethics and integrity, reporting non-compliance, and adhering to applicable federal, state and local laws and regulations, and TVHs policies and procedures. Travel to other sites, including but not limited to patient homes, rehab centers, nursing homes as needed. Attend Investigator meetings and National Research meetings as needed. This position provides on-call and weekend coverage.

EDUCATION:

Bachelor's of Science in Nursing (BSN), preferred. In lieu of BSN, Bachelor's degree with at least 5 years of clinical research experience required.

EXPERIENCE:Minimum five (5) years of clinical research experience; Oncology or cardiology research experience required. Minimum three (3) years preferred of supervisory experience within the last five (5) years.

SPECIAL SKILLS:Ability to analyze research protocols and TVH policies and procedures with respect to implementation and medical, nursing, fiscal, compliance, quality, and risk management aspects. Must have an advanced comprehensive knowledge and understanding of the regulations pertaining to human research protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations), and Health Insurance Portability and Accountability Act (HIPAA). Knowledge of and experience in outpatient and/or inpatient clinical environment, clinical trial regulatory and data submission requirements. Effective written oral and written communications skills. Ability to work independently. Ability to work on teams, and assigned committees. Ability to work in a designated management structure.Area of Talent: Professional AdministrationOrganization: The Valley HospitalDepartment: VH RESEARCH - CLINICAL TRIALSShift: DayFull TimeSchedule: 8am-4:30pmreq16172

United States