Team Lead Pharmacovigilance (m/w/d)

Vality One Recruitment GmbH

  • Festanstellung
089 2152 840 0 jaques.daudert@valityone.com
Vality One ist spezialisierter Personalberater für die Life Science Industrie. Aus dem Herzen Münchens heraus vermitteln wir bundesweit Fach- und Führungskräfte in Direktanstellungen bei unseren Auftraggebern. Dabei decken wir alle Bereiche der pharmazeutischen Wertschöpfung inklusive administrativer Funktionen ab. Sofern Du also Dein Netzwerk innerhalb der Life Sciences erweitern möchtest, sind wir Dein richtiger Ansprechpartner.
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Tätigkeitsbeschreibung:

Dein Aufgabengebiet

  • Lead the global team responsible for pharmacovigilance (PV) operations, offering strategic direction and coaching to team members.
  • Establish and execute strategies for a robust global PV system to ensure operational efficiency.
  • Act as the primary point of contact for cross-functional collaboration on pharmacovigilance operations.
  • Guarantee compliance with international and local reporting obligations for all marketed products and those in development.
  • Implement necessary procedures to enable the PV system to achieve its goals effectively.
  • Regularly liaise with stakeholders in pharmacovigilance and develop quality metrics, including tracking key performance indicators and outsourced PV activities.
  • Coordinate and maintain comprehensive management of PV records and procedural documents to ensure readiness for inspections.
  • Contribute to and oversee internal and external audits related to pharmacovigilance.
  • Facilitate and deliver training on PV-related activities, safety protocols, and compliance processes, covering both clinical and post-market regulatory requirements.
  • Support the PV leadership in designated responsibilities and actively engage in day-to-day activities with a proactive, solution-oriented mindset.

Dein Hintergrund

  • Master’s Degree oder PhD in Pharmacy, Medicine or something other health-care related
  • Extensive knowledge of international drug safety guidelines
  • At least 7 years of experience within international pharmacovigilance
  • MedDRA and AE-coding experience
  • Fluent English-skills

Deine Benefits

  • Familiar environment with plenty of room for development and creativity
  • Top notch working environment: work with like-minded science corpuses
  • Flexible working hours with working time recording and the option to reduce overtime
  • High work-life balance, especially good compatibility of family and career
  • Fully remote position
  • Above-average remuneration with many additional benefits (Christmas bonus, long-term incentive plans, fitness allowance, company pension scheme, training budget, etc.)