Clinical Research Specialist II - Monitoring & Auditing

CEDARS-SINAI

Lancaster, CAFull-timePosted May 4, 2026

Behavioral Health Market Context

Latest national behavioral health workforce report (2026-W22)California behavioral health workforce newsBrowse all behavioral health workforce news
Apply Nowvia Medical Hirings - Talent Rush HQ

Qualifications

  • •While this is a hybrid role, it does require onsite presence for IMVs and audits as needed
  • •Education: Bachelor’s Degree
  • •Work Experience: 5+ years of experience in the area of research specialty of monitoring/auditing

Responsibilities

  • •While this is a hybrid role, it does require onsite presence for IMVs and audits as needed
  • •The Clinical Research Specialist II provides clinical research expertise by participating in the design and implementation of research projects as needed
  • •Responsible for specific and assigned aspects of research infrastructure development, coordinates projects, and communicates status and improvement areas to leadership
  • •May implement and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts
  • •Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB)
  • •Provides clinical research expertise by participating in the design and implementation of research projects as needed by the department or institution
  • •Responsible for specific and assigned aspects of research infrastructure development and/or maintenance
  • •Coordinates research projects at an institutional or departmental level
  • •Communicates project status and improvement areas with leadership in a timely manner
  • •Projects may include, but are not limited to investigator-initiated protocol development including protocol writing, case report form development, budget development, and coordination of departmental research committees
  • •Provides guidance regarding project planning, project logistics, and project implementation
  • •May implement and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts
  • •Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board
  • •Maintains research practices using Good Clinical Practice (GCP) guidelines
  • •Maintains strict patient confidentiality according to HIPAA regulations and applicable law
  • •Participates in required training and education programs
  • •13 more items(s)
Apply for this Position

More Jobs