Pharmacovigilance Agreements Specialist (Valencia / Madrid)

Baxter International; Valencia; Presencial; EUR 40.000 - 55.000; Jornada completa

Descripción de la vacante

A global healthcare company is seeking a Pharmacovigilance Agreements Specialist in Valencia or Madrid to manage safety agreements across multiple countries. The ideal candidate has a background in pharmacovigilance and a Bachelor’s degree in a scientific discipline. This role involves preparing and updating agreements, collaborating with Patient Safety personnel, and ensuring compliance with regulations. The company offers competitive compensation and a focus on work-life balance.

Servicios

Competitive total compensation package

Professional development opportunities

Flexible benefits like childcare vouchers

Work-life balance initiatives

Formación

• Prior background in pharmacovigilance in a pharmaceutical firm.
• Experience in the management of PVAs is preferred.
• Proficiency in written and spoken English.

Responsabilidades

• Preparation and upkeep of Pharmacovigilance Agreements.
• Collaborate with Patient Safety personnel and engage with Third Parties.
• Participate in the review and update of existing PVAs.
• Manage the Global PVA Repository and ensure accurate record-keeping.
• Provide support during internal audits and regulatory inspections.

Conocimientos

Pharmacovigilance knowledge

Project management

Effective communication

Collaboration

Educación

Bachelor’s Degree in a Scientific discipline

Descripción del empleo

Overview

This is where your work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride.

Are you looking to work alongside dynamic and hard-working individuals who are dedicated to saving and sustaining lives? Our team values speed, simplicity, courage, and collaboration in all aspects of our work. Then we would love to hear from you!

Role

We are looking for a Pharmacovigilance Agreements Specialist, either based in Valencia or Madrid, to cover a temporary leave. As a Pharmacovigilance Agreements Specialist, you will have a vital role in safeguarding the safety and efficiency of our healthcare offerings across multiple countries.

What you will be doing

• Preparation, editing and upkeep of Pharmacovigilance Agreements (PVAs), collaborating with country Patient Safety (PS) personnel, and engaging in discussions with Third Parties as needed.
• Working with other collaborators to make sure that relevant business agreements adequately cover Pharmacovigilance (PV) clauses.
• Participating in the regular review and update of existing PVAs to ensure they meet current standards and regulations.
• Ensuring Patient Support Programs (PSP) and Marketing Research Programs (MRPs) are registered in the PSP/MRP Tracking system.
• Managing the Global PVA Repository and the PSP/MRP Tracking system to guarantee accurate record-keeping and adherence to regulations.
• Addressing questions related to PVAs from PS staff and other stakeholders in a timely and accurate manner.
• Providing required PVA documentation and support during internal audits and regulatory inspections to ensure successful outcomes.

What you will bring

• A Bachelor’s Degree or equivalent in a Scientific discipline.
• Prior background in pharmacovigilance in a pharmaceutical firm.
• Experience in the management of PVAs is preferred.
• Proficiency in written and spoken English to effectively communicate with global teams and third parties.
• Ability to partner successfully with cross-functional teams.
• Ability to prioritize tasks and manage multiple projects simultaneously

Why do you want to work at Baxter?

• Competitive total compensation package.
• Professional development opportunities to help you advance your career.
• High importance placed on work-life balance, evidenced by our Family Responsible Certificate (EFR).
• Flexible benefits, including childcare vouchers and employee discounts, to support your personal needs.
• A strong dedication to growing and developing an inclusive and diverse workforce. Baxter Spain holds the DIE certificate "Equality in the Workplace," awarded by the Ministry of Health, Social Services, and Equality since 2016. You can read more about our values at www.baxter.es.

Join us at Baxter and be part of a team that is dedicated to making a difference in the world!

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please let us know the nature of your request along with your contact information.

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