Associate I, Clinical Pharmacology Scientific Support & Reporting
AbbVie · North Chicago
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- Company
- AbbVie
- Location
- North Chicago
- Employment type
- Full-time
- Posted
- September 22, 2026
About this job
To build all necessary data/information needed to prepare internal documents/scientific reports related to clinical trials by assisting with ongoing blinded efficacy and safety reviews. Responsibilities Prepare scientific reports and presentations related to clinical trials using available software and templates. Assists in constructing phase 1 clinical study planning documents, and writes Phase 1 protocols. Comply with procedures set forth in relevant IQS documents and Study protocols Comply with the directives issued by the management regarding clinical studies. Commit to producing work of the highest quality Pay close attention to detail Perform literature and competitive intelligence searches Apply experience to analyze clinical study data, using available software to assist with…
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