Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

People. Passion. Possibilities. Three words that make a world of difference.

More than a job. It's a chance to make a real difference.

Welcome to AbbVie! As part of an international company with 50,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity of addressing some of tomorrows unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global health care? Do you want to contribute to improving patients' quality of life through your expertise? In a challenging work environment that offers opportunities of developing and increasing your own skills? You’ve come to the right place!

As part of the Regional Safety Operations team at the Wiesbaden site, you will be working with talented people and experienced management experts to maintain a high-functioning PV system, enhance our drug safety processes and protect patient well-being.

Together, we break through  – as (Associate) Pharmacovigilance Manager

 

As an (Associate) Pharmacovigilance Manager, you will support the Pharmacovigilance Lead (PV Lead) and the Affiliate Safety Representative (ASR) in all aspects of role and responsibilities, ensuring that the local PV activities and requirements are in line with AbbVie Processes and procedures, the Code of Business Conduct and the local laws.

Make your mark:

 

Your main responsibilities will be as follows:

Safety Science:Support ASR in setting a solid local safety and PV strategy, incorporating proactive PV contributions to ensure a successful product / indication launch at the affiliateBuild strong partnerships and work collaboratively with stakeholders and other functions across the business, such as Regulatory Affairs, Medical Affairs, Brand Teams as applicableMaintain awareness on safety-related product enquiries/issues received from external stakeholders/vendors, working with Medical Affairs, Regulatory Affairs, Area Product Leads and the PSEQ Product Safety Team as required.Involve internal local stakeholders with respect to the results of product safety monitoring, effectively communicating relevant safety information that can impact business strategiesPerform surveillance of Local Safety Information and escalate to Affiliate Medical Director and PSEQ for evaluation on a timely mannerPV System Oversight: Collaborate with Pharmacovigilance and Patient Safety, Epidemiology, R&D Quality Assurance (PSEQ) regional teams and local PV teams to support the PV Lead and the ASR in ensuring oversight of all aspects of the performance and functioning of the PV system in compliance with local regulations, internal company timelines/standards.PV Training: Support the ASR and PSEQ Regional PV Teams in ensuring overall training compliance with corporate procedures and local PV requirements, coordinating the maintenance of the local PV Training matrix and the development and subsequent roll-out of additional PV Training as required (e.g. Risk Minimization Trainings)Perform training activities in the context of AbbVie Employee onboarding, ensuring proper documentationMedical Research Support:Ensure that PV requirements are implemented in all applicable observational studies/Post-Marketing Observational Studies (PMOS) and Investigator-Initiated Studies (IIS).Quality Management:Support ASR and PSEQ Regional teams to ensure quality systems are in place and in line with corporate procedures and local requirements:Collaborate on the creation and maintenance of local PV guidelinesCAPA ManagementSupport the ASR in ensuring that a risk-based Business Continuity plan is in place, allowing for continuation of critical business process for PV; coordinate its testing  Audits and Inspection Management:Support ASR and PSEQ Regional Teams in managing internal PV audits of affiliate service providers/third parties and Regulatory Authority PV Inspections (including corresponding CAPA development and action-tracking to completion in a timely manner)Additional Responsibilities:Coordination of the local PV MailboxSupport in PV Review and Approval of promotional and non-promotional Materials

 

Qualifications

SKILLS

Quality mind-setGlobal view/mind-setGood communicator/influentialExcellent organizational and analytical skills with attention to detailAbility to identify, manage and escalate issues in a timely mannerProcess and operational excellence

EDUCATION/KNOWLEDGE

Academic and/or professional scientific backgroundAdvanced life-science degree (e.g. M.S., M.B.A., PharmD.) preferredRead, write and speak fluent English and German

EXPERIENCE

Minimum 3 years of PV experienceBroad PV systems knowledge Experience in PV case processing, understanding of medical terms, and medical causal relationships, ideally also experience in Signal Management, RMP, DSUR, PSUR compilation and interpretationThorough knowledge of local/regional/area legislation and guidance (clinical trial, pre- and post-marketing)Ideally, experience in Safety Science Strategies and ExecutionChange managementKnowledge of root cause analysis principles

What we offer you:

a diverse work environment where you can have a real impactan open corporate culturean attractive salaryan intensive onboarding process with a mentor at your sideflexible work models for a healthy work-life balancea corporate health management that offers comprehensive health and exercise programscompany social benefitsa wide range of career opportunities in an international organizationtop-tier, attractive development opportunitiesa strong international network
Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html