Patient Safety Lead
Patient Safety Lead
Patient Safety Lead
Patient Safety Lead
Takeda
Pharmazeutische Produkte, Arzneimittel
Wien
- Art der Anstellung: Vollzeit
- 67.000 € – 76.000 € (von XING geschätzt)
- Vor Ort
- Zu den Ersten gehören
Patient Safety Lead
Über diesen Job
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Job Description
Responsible for managing pharmacovigilance (PV) activities in line with Local Operating Companies (LOC) requirements for the DACH region. Supports the development and implementation of processes, systems, and tools for local PV activities, oversees vendor-managed PV tasks. Collaborates with global PV teams, the EU QPPV office, and local stakeholders.
ACCOUNTABILITIES:
- Management of pharmacovigilance (PV) activities according to Local Operating Companies (LOC) requirements for DACH (Germany, Austria, Switzerland incl. Liechtenstein)
- Support the development and implementation of necessary processes, systems and tools for the handling of local PV activities
- Performs oversight tasks of PV activities outsourced to qualified vendors
- Monitors and oversees local Risk Management Plans (RMPs), risk minimization activities, Market Research (MR) and/or Patient Support Programs (PSPs) relevant for the territory
- Reviews protocols for local studies and defines PV related processes for local study projects
- Works with global PV colleagues and the EU QPPV office as well as with local internal stakeholders
- Takes over responsibilities and tasks of:
- deputy Graduated Plan Officer (Stellvertretender Stufenplanbeauftragter) acc. to § 63a AMG and §19 AMWHV for Takeda Germany
- deputy National Appointed Person for Pharmacovigilance acc. to Art. 12 AMBV for Takeda Switzerland
EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:
- Health professional or life sciences degree (Bachelor’s required; advanced degree preferred)
- Minimum of 5 years' advanced experience in pharmacovigilance or related environments
- Meets all applicable local QPPV/PV contact person requirements including education, local language capabilities, training, trustworthiness, and experience
- Advanced experience of working cross-functionally, preferably in R&D companies.
- Understanding of medical/scientific terminology
- Excellent knowledge of PV regulations for the post-marketing global environment and applicable legislation
- Excellent written/oral communication skills in German and English and experience working within virtual teams
- Leadership skills
- Excellent collaborative and organizational skills
- Flexible mindset
- Ability to prioritize under pressure
- High standard of computer literacy
- Execute good documentation practices
- Accuracy and attention to detail
LICENSES/CERTIFICATIONS:
- As required per local QPPV / PV Contact Person requirements, if applicable
- Residency in the European Union
What we offer you:
A competitive remuneration package with a minimum salary of € 5.598,85 gross per month (full-time, collective wage agreement for the chemical industry) - the actual salary is higher and depends on your professional experience and qualifications.
Family-friendly company environment; support with parental leave, dad month, Bilingual company kindergarten
Work@home depending on the position / department
Commuting allowance or parking space (tax applicable)
Comprehensive training programs
In-house job rotation program
In-house Canteen with discounts or meal vouchers
Works council (events, festivals, shopping vouchers, etc.)
Employee Referral Program
Employee Recognition Program
Takeda Resource Groups
Medical checkups
Free vaccination program
Fitness Center in I67
Employee discounts
Employee Stock Purchase Plan
Group accident insurance
LocationsAUT - Wien - Technologiestraße 5AUT - Wien - DC Tower
Worker TypeEmployee
Worker Sub-TypeRegular
Time TypeFull time
Gehalts-Prognose
Unternehmens-Details
Takeda
Pharmazeutische Produkte, Arzneimittel