Literature Review Specialist

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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. 

Purpose:

This position supports the Literature and Vendor Management (LVM) organization to achieve its mission of improving patient lives globally through industry leading safety and compliance by consistent and accurate delivery of high quality, relevant and timely adverse event, medical information, and product quality reports.

In addition, this individual will help shape our culture to help make a remarkable impact on AbbVie customers.

Responsibilities:

• Manages product safety aspects from literature articles:
  • Performs literature review for abstracts and articles received from different sources for AbbVie’s products (all marketed products, late-stage investigational products and relevant drug classes).
  • Identifies other safety information (which might be used in aggregate reports) and potential signals.
  • Manages ordering the relevant full-text articles and translations.
  • Performs EMA MLM daily check.
  • Assists with document archiving, according to internal procedures and current naming conventions.
• Remains current on case processing conventions and regulations.
• Meets company standards for quality, compliance, and productivity.
• Exhibits the Abbvie core leadership attributes: Agile and Accountable; Clear and Courageous; Make Possibilities Real; All for One AbbVie; Decide Smart and Sure.
• Other duties as assigned based on the needs or work requirements of the organization.

Education:

• Bachelor's degree with related health/life sciences background. 

• 1-2 years of pharmaceutical industry experience, including a minimum of 1 year in global pharmacovigilance.
• Demonstrated ability to support project work.
• Ability to handle and prioritize multiple tasks.
• Preferred core knowledge of Industry regulations (ICH, FDA, EMEA, MHRA).

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion.  It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html 

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html