Document & Data QC

New Jersey  ‐ Onsite
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Keywords

Description

RESPONSIBILITIES:
  • Conduct QC review (including verification of data against approved sources) of document deliverables including PSURs, RMPs, responses to regulatory authorities, labels, submission components (SCS, SCE, etc) ensuring accuracy and internal consistency.
  • Provide ongoing analysis of data resulting from the quality review of document deliverables.
  • Collaborate with colleagues in generation of document review metrics.
SKILLS
Quality Control, Regulatory Documentation, Regulatory Experience required. Experience in safety/pharmacovigilance/risk management in the pharmaceutical industry. Knowledge of adverse event report case processing activities so as to ensure the accuracy of ICSR and aggregate data. Knowledge of global regulatory requirements relative to pharmacovigilance, in particular regulatory submission requirements. Demonstrated analytical skills and attention to detail. Demonstrated strength in oral/written communication and interpersonal skills; team player. Demonstrated organizational skills. BS degree; scientific background; healthcare degree/experience preferred. Experience in quality control and/or quality assurance of regulatory submissions/aggregate reports within the pharmaceutical industry highly desirable.

Synectics is an Equal Opportunity Employer.
Start date
n.a
From
Synectics
Published at
30.04.2013
Project ID:
529290
Contract type
Freelance
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