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Company

Global Pharmacovigilance Data Management Manager

Baxter
Marsa, MaltaPosted Discovered via the company's careers siteMatch locked
Full time5+ years exp

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.

Lead a global team. Drive innovation. Make an impact on patient safety worldwide.

Are you an experienced leader who enjoys developing people, solving complex challenges, and turning ideas into effective solutions? Join our Global Pharmacovigilance Data Management team and lead colleagues across Europe, Asia-Pacific and the United States. You will combine people leadership, data and technology expertise, and continuous improvement in a role where collaboration, curiosity and the ability to drive change matter.

WHY JOIN US

•

We foster continuous learning

Build expertise in pharmacovigilance domain, pharmacovigilance regulations, data analysis and automation, while gaining valuable insight into pharmacovigilance systems and technologies. •

We challenge you to grow

You drive your career. We provide a stimulating environment, meaningful challenges, and opportunities that help you reach your full potential. •

We create career opportunities

Explore diverse career paths across PV Technology and broader organization as your interests and expertise evolve. •

We support flexible working

Benefit from flexible working hours and home-office opportunities that help you balance professional and personal priorities. •

We provide global exposure

Collaborate with colleagues across Europe, Asia-Pacific, and the United States, gaining experience in a truly global organization.

WHAT YOU WILL DO

  • Lead and develop a global PV Data Management team.
  • Manage PV Data Management operations.
  • Manage priorities, capacity and resources to ensure timely, high-quality delivery.
  • Develop team capabilities through training, coaching and knowledge sharing.
  • Drive process optimization, automation and sustainable improvements.
  • Partner with PV functions, IT, vendors and other global stakeholders to deliver system and process improvements.
  • Lead and support projects as Project Manager, Technical Lead or Validation Lead.
  • Provide management with meaningful operational insights, KPIs and timely escalation of key risks and issues.

WHAT YOU BRING

  • Strong

people leadership

, with the ability to develop and motivate the team.

  • Strong technical

expertise in PV Data Management

, including pharmacovigilance databases, data models, SQL/PLSQL, reporting and data analysis.

  • Solid

knowledge of pharmacovigilance

, including PV processes and applicable regulatory requirements.

  • Strong

analytical and problem-solving capabilities.

  • Excellent

communication skills

, with the ability to explain complex topics clearly.

  • Strong

planning and organizational skills

, with the ability to manage competing priorities for yourself and others.

  • Curiosity and a

continuous-learning mindset.

  • Experience in

project management

and

report validation

.

EXPERIENCE & EDUCATION

  • University degree in Computer Science, Life Sciences or equivalent with a minimum of 5 years of pharmaceutical industry experience.
  • Experience working with pharmacovigilance databases such as Argus or ARISg and demonstrated experience managing and developing teams.
  • Demonstrated experience managing and delivering projects while achieving defined objectives.

We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The minimum salary for this position is €44,800.00 annually, excluding allowances, overtime and bonuses.

Your initial pay could be at the minimum or higher based on skills and expertise, experience, and other relevant factors, all of which are subject to change. This position may also be eligible for competitive benefits, discretionary bonuses, and/or long-term incentive. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.

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 click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice .

Not included in the source posting: what you'll do.

Skills

sql

Who can apply

The employer didn't state any visa, work authorization, citizenship or clearance requirements in this posting. Confirm with the employer before applying.

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