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Radiant Development (A Division of Radiant Research, Inc.) is a full-service CRO division of Radiant Research. We match your clinical development needs through a complete programmatic assessment: study concept and protocol design, site selection, project management, monitoring, data management, analysis, reports and presentations. Our focus is preventative cardiology, men’s and women’s health, endocrinology, metabolism, and nutrition and functional foods.
We are seeking a full time, highly motivated Clinical Data Coordinator II for our Chicago, IL site. The Clinical Data Coordinator II manually reviews case report forms (CRFs) and output of electronic edit programs according to established data preparation plans; generates, tracks and resolves data queries; follows-up with clinical sites for outstanding queries; reviews and comments on draft case report forms, data management plans, and data preparation plans.
Job Responsibilities include:
Regularly informs Data Manager of overall project status and potential problems
Reviews and comments on draft case report forms, data management plans, and data preparation plans
Writes study specific CRF instructions based on final case report forms
Reviews CRF tracking in order to ensure the presence of all required CRFs and data
Responsible for manual review of CRFs and output of electronic edit programs according to established data preparation plan
Responsible for generation and resolution of data queries
Responsible for tracking queries into the appropriate software programs
Responsible for follow-up with clinical sites for outstanding queries
Participates in Data Management staff meetings
Performs quality control of database as directed
Other duties as assigned
Qualifications:
Required Skills:
Working knowledge of FDA, GCP, and ICH regulations specific to data management for clinical studies
Understanding of medical terminology and familiarity with standards of care and disease states
Well organized, with strong attention to detail and excellent analytical ability
Excellent interpersonal, communication and problem solving skills, excellent command of the English language, both oral and written
Able to meet critical milestones and timelines
Able to manage all assigned tasks efficiently and effectively, able to work on multiple tasks simultaneously
Adaptable to changes in work duties, responsibilities, and requirements
Proficient with Microsoft Word and Microsoft Excel, experience with ClinPlus data management system preferred
Experience:
2+ years as a clinical data coordinator, clinical research coordinator and/or monitoring experience
Education:
Bachelor’s degree in a related discipline or equivalent experience
We offer a competitive benefits package with medical, dental, and vision coverage, life and disability insurance, and 401K. Radiant Research is an Equal Opportunity Employer.
If you are interested in applying, please e-mail your resume to careers@radiantresearch.com or fax
it to 513-530-8551
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