Pharmacovigilance Associate

Location: Bayern, Deutschland Salary: Verhandelbar
Sector: Life Sciences Type: Temporary

Dear pharmacovigilance colleagues,

I hope you are well and enjoying the beautimus sun as I am.

I would like to offer you the following work opportunity as:

DRUG SAFETY ASSOCIATE, for my client in Bavaria, Germany.

By interest, take a look at the expectations and contact me for further details. If you do not have free capacities, feel free to pass it along:

Pharmacovigilance Associate (m/w)

Project expectation:

  • PV documentation administration, including the forwarding of incoming data of adverse effects and data entry
  • Organizing and monitoring of case processing with continuous focus on deadline hold and work precision
  • Forwarding of all adverse effects to the respective regulatory authorities und licensed partners as well as internal business partners from other key areas
  • Daily development and processing of PV-lists in order to confirm case standing and completion of all AEs
  • Filing and archiving of relevant PV-documents
  • Reconciliation of drug risk reports in cross-functional form

Background expectation:

  • Fulfilled Degree / Certification in Medical Documentation, Medical Assistance or relatable pharmaceutical / scientific education ex. PTA or Nurse
  • Experienced in the pharmaceutical industry or relatable industry of advantage
  • Good knowledge of medical terminology, ideally in MedDRA coordination
  • Good skills in MS Office
  • Fluent German with good English speaking skills

Start: June 2018

Location: Bavaria

Duration: 7 month (possible extension TBD)

Hiring model: ECM, fulltime and on-site

Thank you for your consideration, looking forward to your application and a possible mutual collaboration,


Charlotte Valentiner

Senior Recruitment Consultant

Medical Affairs / Market Access / Drug Safety - Freelance

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