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Job

Pharmacovigilance Manager

  • Location

    Darmstadt

  • Sector:

    Life Sciences

  • Job type:

    Permanent

  • Contact:

    Sandeep Bains

  • Contact email:

    s.bains@hamlynwilliams.com

  • Salary high:

    0

  • Salary low:

    0

  • Published:

    about 1 month ago

  • Expiry date:

    2022-06-19

  • Startdate:

    ASAP

Hamlyn Williams has partnered with a rapidly expanding global pharmaceutical company based in Darmstadt, Germany. This global pharmaceutical firm is currently in a major phase of growth due to its innovative and expansive pipeline and are looking for a Pharmacovigilance Manager on a permanent basis.

This role can be remote with flexible approach to office travel and paid commuting cost. This role will be supporting Global QPPV Office in the management of the Pharmacovigilance System Master Files (PSMFs).

The role will involve but not be limited to: 

  • Oversee adherence to the global guiding principles to harmonize the processes of local PV system file (or similar concepts) maintenance by the relevant company affiliates worldwide as applicable. Oversee the maintenance of local PV system files by the relevant local teams.
  • Support the Global QPPV and the relevant Global PV organisation to maintain a framework for Local Person responsible for Pharmacovigilance (LPPV) collaboration and alignment.
  • Work with Global QPPV to improve overview of the Global PV system.
  • Manage all routine activities and the Global QPPV office mailbox in collaboration with the relevant Global QPPV office team members.
  • Support any other initiatives by Global QPPV office and Global Pharmacovigilance team.
  • Partner with stakeholders across multiple functional lines globally to ensure high quality contributions delivered in a timely manner.
  • Collaborate with stakeholders in relevant continuous improvement activities.

As a Regulatory Affairs Associate, you will need:

  • Three years of experience in pharmacovigilance or clinical safety; experience with project management is also beneficial. 
  • Understanding of the processes associated with Pharmacovigilance and Regulatory or Clinical Development
  • Experience in coordinating and editing large, complex documents with multiple contributors with tools and systems that include document management, records management, data visualization

I am a market expert in the Pharmacovigilance area working with a large variety of clients across the pharmaceutical and biotechnology industries. If this role is of interest to you, or if you’d like to explore other opportunities in the market, please feel free to reach out directly. Contact Sonny Bains at +44 020 8164 5340 or at s.bains@hamlynwilliams.com.