• Job Description

  Req#: JR - 118121

  This is where you save and sustain lives

  At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

  Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

  Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

  Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.

  As the Pharmacovigilance Specialist for the UK and Ireland you will be responsible for (in collaboration with the Pharmacovigilance Manager), to maintain an efficient local Pharmacovigilance system in the UK and Ireland meeting the European and national regulations and in compliance with the Baxter Pharmacovigilance procedures. To ensure appropriate contacts with the other organizations not limited to country Regulatory Affairs, Country Quality Assurance, Quality Assurance, Business Units and with HCP and Competent authorities (HPRA and MHRA).

  To work closely with the PV Nordic colleagues based in Nordic according to the cluster model and provide back-up activities as needed.

  To cooperate with DACH colleagues and provide back-up activities for DACH cluster in terms of ADR reporting - MUST be able to speak German

  Currently the team come to the Newbury office once a week.

  You would be accountable and responsible for the following activities :

  1. Local PV system

  2. ADR Reporting

  3. Clinical trials activities

  4. Agreements with third parties

  5. Training

  6. PSURs, RMPs, PASS, PSP/MRPs

  7. Regulatory intelligence

  8. Audits and inspections

  9. Compliance

  10. Other local PV activities

  11. Activities related to associated countries in the cluster

  Knowledge or skills gained through a combination of academic study (requires a degree in Medicine, or Pharmacy or in Life Science. A degree in Pharmacovigilance or Toxicology or Pharmacology or Immunology would be an asset)

  Ability to communicate efficiently verbally and in writing.

  Structured and organized approach to work.

  Ability to write and discuss medical documentation.

  Ability to use computerized applications and systems and especially Global PV Database.

  Ability to liaise with the different functions i.e., Global Pharmacovigilance, Regulatory Affairs, Country Quality Assurance, businesses, Legal Affairs.

  Ability to communicate efficiently verbally and in writing in German language.

  What are some of the benefits of working at Baxter?

  • Competitive total compensation package

  • Professional development opportunities

  • High importance is placed on work-life balance

  • Commitment to growing and developing an inclusive and diverse workforce

  #ind-ukops

  #IND-UKOPS

  Reasonable Accommodations

  Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to Americas_TTA@baxter.com 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.

• About the company

  Baxter International Inc. is an American multinational health care company with headquarters in Deerfield, Illinois.

Notice