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Clinical Data Associate
| Details |
Country: USA
Location: Illinois-Chicago North Deerfield, IL 60015
Total applied: 42 Job Category:Biotech/R&D/Science
Relevant Work Experience:2+ to 5 Years
Education Level:Bachelor's Degree
Location:Deerfield, IL 60015
Status:Full Time, Temporary/Contract/Project
Occupations:Clinical Research;Mathematical/Statistical Research;General/Other: R&D/Science
Career Level:Experienced (Non-Manager)
Relevant Work Experience:2+ to 5 Years
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Clinical Data Associate
Pharmaceutical Company known for it's favorable work environment is in need for a Clinical Data Associate for a long term contract opportunity. This position is located in Deerfield, IL. Competitive compensation, benefits available. We are looking to fill this position immediately!
2 positions available: one with 1+ years of experience and one with 4+ years of experience.
RESPONSIBILITIES:
We are looking for an experienced Data Manager with the following:
Preferably >5 years Data Management experience
Experience in Managing Projects
Experience in EDC
DATA COLLECTION
· Collaborates with Clinical to finalize CRF design
· Annotates CRFs properly
· May be required to design user interface using optical character recognition (TELEform) or web-based electronic data capture technology (EDC)
· Collaborates with IS to establish the clinical database setup
DATA CLEANING
· Develops, implements and maintains Data Prep Plan with input from Medical, Clinical and RDO
· Programs and tests computer diagnostic edit checks
· Prepares data listings for use in CRF review
· Reviews CRFs for data issues and inconsistencies
· Issues Requests for Information (RFI) and verifies subsequent responses in the clinical database
· Interacts regularly with study team regarding CRF review and completion procedures
· Participates in data review meetings by identifying potential issues
· Performs required steps to lock databases
DATA CODING
· May be required to code and/or maintain coding dictionaries for adverse events and/or medications, such as MEDdra and WHODRUG
ADMINISTRATION
· Participates in study team and all related meetings for assigned protocols by providing DM status reports
· May be required to develop study timelines for DM milestones in conjunction with study team
· May be required to train others in DM processes
· May be required to train others and/or implement new technologies
· May be required to travel for project meetings and site training purposes
DIMENSIONS:
· Must ensure that databases meet requirements of clinical projects.
· Requires knowledge and understanding of the data management process to facilitate timely data review and processing.
· Must possess excellent communication skills in order to work with personnel in other departments to ensure the successful completion of clinical trials databases.
For immediate consideration, please contact:
Chip Holway
847-374-8250 x239
cholway@delta-pharma.com
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