Additionalinformation

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

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Companydescription

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn,Facebook, Instagram, X and YouTube.

Jobdescription

Job Description

This position is contributing to world-wide surveillance of clinical trial patient safety data and continuous improvement efforts. Core Job Responsibilities include:

• Provides timely assessment of reported clinical trial data and participates in applicable safety
• surveillance activities for assigned studies including review and contribution to ad-hoc Safety Reports
• as needed.
• Provide review and analysis of safety-related data from clinical trials for content, quality, potential
• study level trend identification, and adherence to regulatory guidance and protocols utilizing critical
• thinking skills.
• 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
• investigator sites as needed.
• Participates in review of study protocols to ensure appropriate safety language.
• Review safety sections of the clinical study reports, and other ad-hoc reports which include safety
• data.
• Creates narratives of serious adverse events and other identified events of interest in accordance with
• accepted standards.
• Current with knowledge of ICH, FDA, and EMA regulatory guidance’s affecting safety surveillance.
• May serve on departmental process improvement projects.
• Supports department, division and company's strategic direction by demonstrating the AbbVie “Ways
• We Work” leadership behaviors.

Qualifications

• Bachelor's degree with related health science background. RN or clinical pharmacy experience strongly preferred.
• A minimum of 2 years’ experience to include at least 2 years of clinical practice experience and a preferred 1-year drug safety experience with clinical trial life cycle management – Pre-clinical to Phase III through launch to market.
• Proficiency in Computers (Windows, Word, Excel) and in specific databases (e.g., oracle/clinical, PIMS, laboratory databases).
• Ability to critically evaluate medical data understanding the clinical course and treatment modalities.
• Effective communication skills in delivering study-related information.