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CLINICAL RESEARCH COORD II - CRI MED Hem Onc 900 Cent Blvd

Apply Job ID 44030 Job Status Full Time Shift 1

More information about this job:


Short Description:


Assists 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.

Special Requirements:


Scheduled Days / Hours: M-F

Education:

Bachelors Degree preferred.

Experience:

Minimum 3-5 years of research experience required.

Required License/Certifications/ Registration:

CRCC preferred.

Other Qualifications:

Basic understanding of Microsoft Excel, Outlook and Word.

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  • Professionals, Camden, New Jersey, United StatesRemove