Specialist, Pharmacovigilance Operations - Warszawa

Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. · Reviewing ranking verifying processing and documenting case-related inf ...

Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology. · Best-in-class healthcare, · a holistic approach to well-being with access to fitness, mindfulness, and mental health support, · family buildin ...

If you're interested in this role, please apply in English and include an English version of your Resume/CV. · If you're interested in this role, please apply in English and include an English version of your CV. · The Role · Reporting to the Director, PV Operations – Case Proces ...

We are seeking a Pharmacovigilance Operations Specialist to join our team in Warsaw. As a key member of our PV Operations – Case Processing team, you will be responsible for effective execution of activities related to triage, processing and quality control of individual case saf ...

We are seeking a Head of Affiliate Regulatory & Pharmacovigilance to lead all regulatory affairs and pharmacovigilance activities for our CEERTMEA operations. · ...

This role involves managing regulatory activities for products and medical devices throughout their lifecycle. · ...

At Elanco (NYSE: ELAN) we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. · Regulatory Strategy & Execution: Develop, implement, and manage comprehensive CEERTMEA regulatory strategies for the lifecycle manag ...

· Company Description · We are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all c ...

+ Pharmacovigilance Officer Team Leader Leads the team responsible for ICSR management for a selected project or group of projects as Team Leader  · Ensures adequate distribution of tasks for assigned projects and teams and oversees the workflow process  · ...

Working with Us · Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production lin ...

Working with Us · Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production lin ...

Position Purpose · The QPPV Compliance Director supports the activities of European Union Qualified Person for Pharmacovigilance (EUQPPV) and the European Safety Office and guarantees the oversight of the quality and compliance of the Pharmacovigilance system. · Primary Responsib ...

+ Job summary: The Senior Specialist collaborates with cross-functional colleagues to support operational regulatory pharmacovigilance company policies, processes, standards and software system configuration that impact individual case safety reports, aggregate reports and downst ...

Working with Us · Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production lin ...

The Senior Specialist collaborates with cross-functional colleagues to support operational regulatory pharmacovigilance company policies processes standards and software system configuration that impact individual case safety reports aggregate reports and downstream medical revie ...

To provide strategic and operational Medical Affairs leadership with oversight of Pharmacovigilance (PV) activities across the region ensuring full compliance with EU and local regulatory requirements while maintaining the highest standards of scientific integrity patient safety ...

The Client Quality Manager is primarily responsible for implementing and maintaining the quality system and training for assigned client projects. · ...

The SERM Scientific Director will provide in-depth medical/scientific expertise in the safety evaluation and risk management of key GSK assets or in clinical development and/or the post-marketing setting. Ensures scientifically sound review and interpretation of data and manageme ...

Working at Bristol Myers Squibb involves challenging work with opportunities for growth and development. Employees have access to competitive benefits and services. · ...

The SERM Scientific Director will provide in-depth medical/scientific expertise in the safety evaluation and risk management of key GSK assets or in clinical development and/or the post-marketing setting. · ...

The Pharmacovigilance Physician will provide medical and clinical expertise to ensure robust safety surveillance across all Theramex products. · ...