Clinical Trials/ Research Super

Area of Talent: Nursing
Organization: The Valley Hospital
Department: VH RESEARCH – CLINICAL TRIALS
Shift: Day
Status: Full Time
Job Description:
POSITION 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.

Certifications and Licenses: Current NJ RN license preferred. Current BLS
certification preferred. Current IATA/DOT certification preferred. CCRP or CCRA certification preferred and willingness to obtain other certifications, if
required.

Location: Ridgewood, NJ

Returning Applicants

Login to check your application history, set up or edit job agents, or to update your profile.