Business Analyst

Recruiter
Parity Professionals
Location
Welwyn Garden City
Salary
£275 - £300 daily
Posted
05 Jul 2018
Closes
19 Jul 2018
Position/Level
Professional / Specialist
Sector
Technology
Contract Type
Contract / Interim
Language
English

Business Analyst

Business Analyst/Pharma/Welwyn Garden City/12 Months/300pday

Looking for a Business Systems Analyst to be a key member of the Pharmacovigilance Information and Systems (PVIS) group.

Primary Responsibilities and Accountabilities:

  • Provides change management, master data maintenance and front-line application support for applicable Drug Safety systems on behalf of PDS
  • Performs global safety database activities, global regulatory submission activities, basic safety data searches and reporting
  • Content management using information management tools like DSO and QTT
  • Assesses, evaluates and implements technology enhancements to support global and local business processes
  • Interacts with Drug Safety functional groups, other information management functions in Development, IT organizations, external business partners, vendors and health authorities
  • Represents the PVIS group in department and cross-functional initiatives
  • Creates or reviews requirements, specifications and business process documentation
  • Designs logical and innovative solutions to complex problems
  • Participates in global, cross-functional activities and projects, ie within PDS, as well as affiliates and other PD functions
  • Provides support, administration and change management for existing Drug Safety systems
  • Maintenance of the systems' Master Data (ie business configuration) such as user account management, regulatory reporting rules, document templates, protocols, drug dictionaries
  • Acts as a process owner for Master Data activities and works closely with the management team to ensure that the process remains effective and works efficiently
  • Ongoing review of PV Information and Systems processes to provide suggestions for continuous improvement

Experience, Skills, Knowledge:

  • Drug Safety knowledge or other relevant experience in the drug development environment within the pharmaceutical industry
  • Experience in Individual Case Systems Reporting (ICSR)
  • Knowledge of drug safety regulatory obligations and guidelines
  • Working knowledge of medical terminologies, eg MedDRA
  • Experience in user acceptance testing
  • Working knowledge of industry standard safety systems

For more information please send in your CV.

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