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Clinical Research Coordinator I

2 months ago


Camden New Jersey, United States Cooper University Hospital Full time

About Us:

At Cooper University Health Care, our commitment to providing extraordinary health care begins with our team of dedicated professionals. Our team is continuously discovering clinical innovations and enhancing access to the most up-to-date facilities, equipment, technologies, and research protocols.

We have a commitment to our employees by providing competitive rates and compensation, a comprehensive employee benefits program, attractive working conditions, and the opportunity to build and explore a career by offering professional development.

Our team is passionate about delivering exceptional patient care and advancing medical research. We strive to create a work environment that is collaborative, inclusive, and supportive of our employees' growth and development.

Job Summary:

The Clinical Research Coordinator I will assist the Principal Investigator and other members of the research team with the preparation of IRB protocols, consent forms, and development of study budgets. This role will also involve completing and maintaining all study documents as required, identifying and recruiting study participants, and working collaboratively with the research team.

Key Responsibilities:

  • Assist the Principal Investigator and research team with the preparation of IRB protocols, consent forms, and study budgets.
  • Complete and maintain all study documents as required, including participant consent forms and study protocols.
  • Identify and recruit study participants, ensuring that all necessary documentation is completed and maintained.
  • Work collaboratively with the research team to ensure the successful completion of studies.

Requirements:

  • 0-2 years of research experience.
  • Medical Assistant, LPN, or Phlebotomist experience preferred.
  • High School Diploma or Equivalent required.
  • Basic understanding of Microsoft Excel, Outlook, and Word.