Keep the discussion going--join our JobWatch Group on LinkedIn!

Sign In
 [New User? Sign Up]
Mobile Version

Clinical Trials and Research Supervisor

Valley Health System of Ridgewood

Ridgewood, New Jersey
  • Clinical Operations
Valley Health System of Ridgewood
  • Save Ad
  • Email Friend
  • Print
  • Research Salary

Job Details


The Supervisor, Clinical Trials and Research Unit (S-CRTU), position is responsible for the administrative leadership, daily operations and clinical conduct of their assigned clinical trials and research unit(s) of The Valley Hospital (TVH), i.e., cardiology, oncology, neurology etc. This position is also responsible for oversight of all clinical activities that are part of research studies and participates as a main coordinator on studies. The position is also responsible for oversight of all clinical and non-clinical research personnel in a manner that effectively maximizes efficiency, quality and compliance with clinical research standards, patient safety, and staff satisfaction. Effectively manage staff, budget, resource/allocation planning, and performance assessments for a variety of clinical, regulatory and research functions. Consistently supports compliance and TVH’s Code of Conduct and S.E.R.V.E. values by maintaining the privacy and confidentiality of information, protecting the assets of the organization, acting with ethics and integrity, reporting non-compliance, and adhering to applicable federal, state and local laws and regulations, accreditation and licenser requirements (if applicable), and TVH’s 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.



Bachelor’s of Science in Nursing



One year of Molecular Diagnostics laboratory experience preferred. Must be eligible to be certified in Molecular Pathology (ASCP) and attain this certification within one year.



Ability to analyze research protocols and TVH policies and procedures with respect to implementation and medical, nursing, fiscal, compliance, quality, and risk management aspects. In-depth working knowledge of nurse practice act, GCP, federal, state, and local regulations including HIPAA and TVH policies and procedures. 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.

Powered ByLogo