Clinical Data Associate

Job Responsibilities

• Gain experience with MS Office applications
• Learn ICH guidelines, 21 CFR Part 11, ISO 9001 and ISO 7001.
• Gain exposure to eCRFs, CRF Completion Guidelines, Edit check specs, and DMP
• Contribute to study tracking and metric reports for use by the study team
• Contribute to user acceptance testing (UAT) of EDC and integrated systems including execution of test plan and scripts.
• Member of project team.

Job Requirements

• Bachelor's Degree in a scientific, medical, or clinical discipline or related field is required; Master's or PhD preferred
• 1-2 years of previous experience in clinical data management
• Hands-on experience with clinical trials and pharmaceutical development preferred
• Experience in the pharmaceutical or CRO industry must
• Experience with query and discrepancy management required
• Has a strong attention to detail

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