Cooper University Health Care
Clinical Research Coordinator II
Cooper University Health Care, Camden, New Jersey, United States, 08100
About UsAt
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 its 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 DescriptionAssists the Principal Investigator and other members of the research team with preparation of IRB protocols, consent forms, and development of study budget.
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 RequiredMinimum 3-5 years of research experience required.
Education RequirementsBachelors Degree preferred.
License/Certification RequirementsCRCC preferred.
Special RequirementsBasic understanding of Microsoft Excel, Outlook and Word
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 its 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 DescriptionAssists the Principal Investigator and other members of the research team with preparation of IRB protocols, consent forms, and development of study budget.
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 RequiredMinimum 3-5 years of research experience required.
Education RequirementsBachelors Degree preferred.
License/Certification RequirementsCRCC preferred.
Special RequirementsBasic understanding of Microsoft Excel, Outlook and Word