
Clinical Safety Analyst
Participates in applicable safety surveillance activities for assigned products; and in planning and completion of Ad-Hoc Safety Reports as needed. Timely assessment of adverse event coding for consistency and accuracy of coding and ; accurate and effective medical review of safety-related CRFs and labs, including communication with Study Designated Physicians Supervise tracking of safety -related queries to Investigators and assists in handling safety questions from IRB/IEC. Create narratives of serious adverse events and other identified events of interest in accordance with accepted standards and with high degree of competency. Does not initiate strategic decisions, but is responsible for supporting the department, division and company's strategic direction. Starts to mentor/teach others with directions from lead mentor or team manager. Assists in mentoring staff by coaching and mentoring designated Safety staff on assigned safety activities.
Minimum 3 years clinical experience
A minimum of 1 year drug safety/pharma experience
Ability to critically evaluate medical data.
Analyze and interpret adverse event data as a component of clinical surveillance activity.
MS Word
MS PowerPoint
Time Management Skills
MS Excel skills
Verbal communication
Prioritizing skills
written communication
Self-Motivated
Flexibility/Adaptability
Detail Oriented and Organized
multitasker
According to JobzMall, the average salary range for a Clinical Safety Analyst in 1 N Waukegan Rd, North Chicago, IL 60064, USA is $95,000 to $110,000 per year. This range can vary depending on experience, qualifications, and the specific job requirements.
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AbbVie is an American publicly traded biopharmaceutical company founded in 2013. It originated as a spin-off of Abbott Laboratories.

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