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Children's Memorial Hospital
Location: Chicago, IL 60601 Document ID: A4024-0FX0 Posted on: 2010-05-0305/03/2010 Job Type: RegularJob Schedule:Full-time
2010-06-02
Clinical Research Coordinator, Sr.
This position coordinates multiple and/or more complex clinical research protocols.
ESSENTIAL JOB FUNCTIONS:
- Verifies and recruits subject eligibility and study subjects. Conducts consent/assent procedures and clinical research visits.
- Prepares personnel and study materials for training, recruitment, enrollment, and follow-up. Prepares protocols, informed consents, amendments, SAE reports, and other necessary documents for review by the IRB and sponsor. Prepares and maintains all records and files required by regulatory agencies and sponsors.
- Assists with training of staff and provides oversight of study charges to fund accounts
- Assists in statistical analysis.
- Collaborates on the preparation of abstracts/posters for scientific meetings and manuscripts for publication.
FTE status: FT-80
Requirements
- Certification as a Clinical Research Professional (SOCRA) or Clinical Research Coordinator (ACRP) required
- Master's degree in a related field, or, Bachelor's degree with 3-5 years experience in clinical research, or, Minimum of 2 years experience as a CRC II; coordinating multiple and/or more complex research protocols
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