What are the responsibilities and job description for the CLINICAL RESEARCH COORDINATOR II position at Cooper University Health Care?
About Us
At Cooper University Health Care, our commitment to providing extraordinary health care begins with our team. Our extraordinary professionals are continuously discovering clinical innovations and enhanced 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 programs, attractive working conditions, and the chance to build and explore a career opportunity by offering professional development.
Discover why Cooper University Health Care is the employer of choice in South Jersey.
Short Description
Assists the research manager, principal Investigator, and other members of the research team with preparation of IRB protocols, consent forms, data entry, and other tasks as needed.
Completes and maintains all study documents as required.
Assists with the identification and recruitment of study participants.
Work as a team player with all involved in the studies.
Experience Required
Minimum 3-5 years of research experience required.
Education Requirements
Bachelors Degree preferred.
Special Requirements
Basic understanding of Microsoft Excel, Outlook and Word.
At Cooper University Health Care, our commitment to providing extraordinary health care begins with our team. Our extraordinary professionals are continuously discovering clinical innovations and enhanced 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 programs, attractive working conditions, and the chance to build and explore a career opportunity by offering professional development.
Discover why Cooper University Health Care is the employer of choice in South Jersey.
Short Description
Assists the research manager, principal Investigator, and other members of the research team with preparation of IRB protocols, consent forms, data entry, and other tasks as needed.
Completes and maintains all study documents as required.
Assists with the identification and recruitment of study participants.
Work as a team player with all involved in the studies.
Experience Required
Minimum 3-5 years of research experience required.
Education Requirements
Bachelors Degree preferred.
Special Requirements
Basic understanding of Microsoft Excel, Outlook and Word.
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