Clinical Safety Analyst at AbbVie

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Provides timely assessment of reported clinical trial data and participates in applicable safety
Provide review and analysis of safety-related data from clinical trials for content, quality
Maintains constant state of audit readiness for study deliverables.
Monitoring of safety-related queries to Investigators.
In collaboration with medical monitor, plans and executes the plan for study safety review.
Provides safety overview to the clinical team, Clinical Research Organizations, Investigators and

Bachelor's degree with related health science background. RN or clinical pharmacy experience
A minimum of 2 years’ experience to include at least 2 years of clinical practice experience and a
Proficiency in Computers (Windows, Word, Excel) and in specific databases (e.g., oracle/clinical
Ability to critically evaluate medical data understanding the clinical course and treatment
Effective communication skills in delivering study-related information.
Fluency in Japanese and business-level English, with the ability to communicate effectively with

Clinical Safety Analyst