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Job Details
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Pharmacovigilance Specialist- 6 month contract



Business Type: Pharmaceutical Company, Clinical Research Organisation, Contract Research Organisation, Pharmaceutical Services
Job Type: Pharmacovigilance
Job Level: Experienced (non manager)
Position: Full Time
Location: Poland
Reference: NS3567
Closing Date: 18/06/19
Job Details:

Pharmacovigilance Specialist

Sector: Pharmacovigilance and Medical Information

Contract- 6 months

Location: Poland

Salary: Lucrative hourly rate

Start date: Immediate

INTRO:

A top global CRO company is currently on the search for an ambitious candidate who is looking to build a career within the pharmacovigilance industry. This company is the largest provider of biopharmaceutical development and outsourcing services conducting business in approximately 100 countries.

This position requires the candidate to review, assess and process lifecycle safety data information across all services which is received from a variety of sources. The candidate will distribute reports/data to both internal and external third parties following SOPs and guidelines.

REQUIREMENTS:

  • Degree in a relevant science subject or Diploma with relevant experience
  • Ability to manage multiple workloads and prioritisation
  • Resilience
  • Excellent attention to detail
  • Must be a good team player
  • Excellent communication skills
  • 2-3 years experience in drug safety
  • Must be organised

RESPONSIBILITIES:

  • Receive, triage, review and process data from various sources on time within budget, meeting quality standards.
  • Medical information tasks
  • Performing data entry for tracking using the safety database
  • Coding relevant medical terminology
  • Narrative writing
  • Generating queries
  • Quality control
  • Reconciliation tasks
  • Coordinating translations
  • Preparation of materials for submission of primary review
  • Receive and document incoming telephone calls, faxes and e-mails from investigative sites reporting Lifecycle Safety data.
  • Processing Lifecycle Safety data according to regulations, guidelines and SOPs.
  • Assisting the operations team with tasks such as generations of status reports and providing metrics
  • Liaising with a variety of functional teams- clinical, data management, health care professionals
  • Attending project team meetings and providing feedback to the Operations Manager

To Apply

If you would like to discuss this vacancy further, please call i-Pharm Recruitment Consultant Niki Sansoy on +44 (0)20 3189 0470

ABOUT i-PHARM CONSULTING

i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.



Posted: 21/05/2019 | NPJ Ref: 235965
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