drjobs Literature Review Specialist (maternity replacement)

Literature Review Specialist (maternity replacement)

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1 Vacancy
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Job Location drjobs

Bucharest - Romania

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

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 AbbVies 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.

Qualifications :

Education:

  • Minimum: A degree with related health/life sciences background RN BSN BS BS Pharm. Candidates lacking the appropriate degree but with previous pharmaceutical experience may be considered.

Experience:

  • 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).


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. 

US & Puerto Rico only - to learn more visit  & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

No


Employment Type :

Full-time

Employment Type

Full-time

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