Clinical Research Specialist I - Gastroenterology and Hepatology Division/Depart

Clinical Research Specialist I - Gastroenterology and Hepatology Division/Department of Medicine at CEDARS-SINAI summary:

The Clinical Research Specialist I in the Gastroenterology and Hepatology Division is responsible for coordinating research projects, ensuring compliance with regulatory standards, and contributing to the design and implementation of clinical trials. This role requires collaboration with researchers and doctors to enhance patient care through groundbreaking studies in digestive and liver diseases. The specialist maintains research practices according to Good Clinical Practice guidelines while communicating project status and updates to leadership.

Are you looking to contribute to groundbreaking research? We look forward to having you join our team to collaborate on groundbreaking research!

About the Role

As a Clinical Research Specialist I, you will provide clinical research knowledge by participating in the design and implementation of research projects as needed. This position is responsible for specific and assigned aspects of research infrastructure development, coordinates projects, and communicates status to leadership.

About the Team

Researchers and doctors in our Division of Gastroenterology and Hepatology continue to be at the forefront of groundbreaking tests and treatments for all types of digestive and liver diseases, while driving groundbreaking research to improve patient care.

Primary Duties and Responsibilities:

• 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.

Education:

• Bachelor's degree is required.

Experience:

• Three years of proven experience in area of research specialty.

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Keywords:

Clinical Research, Gastroenterology, Hepatology, Patient Care, Research Coordination, Clinical Trials, Good Clinical Practice, FDA Compliance, Medical Research, Patient Confidentiality