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Clinical Research Coordinator I

2 months ago

Los Angeles, California, United States CEDARS-SINAI Full time
Position Overview

The Smidt Heart Institute exemplifies Cedars-Sinai's unwavering commitment to cardiovascular health and pioneering research, providing patients with access to top-tier medical care. Each year, countless individuals place their trust in the Smidt Heart Institute at Cedars-Sinai. Our team of cardiologists, cardiac surgeons, and specialized healthcare professionals address a comprehensive range of heart conditions, while our researchers strive to push the boundaries of medical science through innovative and life-saving studies. From genetic counseling to advanced therapeutic options, Cedars-Sinai remains at the leading edge of technology and discovery, enhancing patient outcomes.

Become a part of our esteemed team and leverage your expertise within a nationally recognized research institution.

The Clinical Research Coordinator I plays a vital role in providing clinical research knowledge by engaging in the planning and execution of research initiatives as required. This position is accountable for designated components of research infrastructure development, overseeing projects, and effectively communicating progress and areas for enhancement to management. Responsibilities may include the implementation and coordination of organization-wide initiatives such as research quality assurance or clinical trial participant recruitment. This role ensures adherence to all federal and local regulations, including those set forth by the Food and Drug Administration (FDA) and local Institutional Review Board (IRB).

Key Responsibilities

  • Contributes clinical research expertise by engaging in the planning and execution of research initiatives as required by the department or organization.
  • Accountable for specific and designated components of research infrastructure development and/or maintenance.
  • Oversees research projects at either an institutional or departmental level.
  • Effectively communicates project progress and areas for improvement with management in a timely manner.
  • Projects may encompass, but are not limited to, investigator-initiated protocol development, including protocol drafting, case report form creation, budget formulation, and coordination of departmental research committees.
  • May implement and coordinate organization-wide initiatives such as research quality assurance or clinical trial participant recruitment.
  • Ensures compliance with all federal and local regulations, including those established by the Food and Drug Administration (FDA) and local Institutional Review Board.
  • Maintains research practices in accordance with Good Clinical Practice (GCP) guidelines.
  • Upholds strict patient confidentiality in compliance with HIPAA regulations and applicable laws.
  • Participates in mandatory training and educational programs.

Qualifications

Educational Background:

  • A minimum of a Bachelor of Science or Bachelor of Arts degree in biological sciences is required.

Professional Experience:

A minimum of 3 years of experience in the relevant area of research specialty is required.


Job ID : 1983
Working Title : Clinical Research Coordinator I - Cheng Lab, Heart Institute
Department : Heart Institute
Business Entity : Cedars-Sinai Medical Center
Job Category : Academic / Research
Job Specialty : Research Studies/ Clinical Trials
Overtime Status : EXEMPT
Primary Shift : Day
Shift Duration : 8 hours
Base Pay : $52.92