Req # JR – 039110
Location Søborg, Capital Region, Denmark
Job Category Patient Safety
Date posted 04/26/2021
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.
Summary
Our fantastic Pharmacovigilance Associate in Denmark is going on Maternity leave in August, so this is a great opening for you who easily embrace a new role in a complex organization. The assignment is for a period of 14 months.
You will be a part of an important support function as a Pharmacovigilance Associate in Denmark. You will interact and promote Pharmacovigilance internally and collaborate with the Pharmacovigilance Director, and your team in Sweden and UK & Ireland. You will maintain an efficient Pharmacovigilance system meeting the European and national regulations and secure the compliance with the Baxter Pharmacovigilance procedures.
Essential Duties and Responsibilities
- To collect, document, follow-up all local AEs and other pharmacovigilance information (e.g. pregnancy, medication error, lack of efficacy) from all sources according to SOPs.
- To provide appropriate training on PV to new employees, HCP facing employees, partners and vendors.
- To implement global Pharmacovigilance SOPs, to create and update local Pharmacovigilance related procedures.
- To support the EMEA PV Agreement team in the implementation of local PSPs/MRPs.
- To closely monitor local compliance, open non-conformance reports as appropriate and help in the resolution.
- To ensure all efforts are made to achieve high compliance rates.
Qualifications
- In this role you can be a newly graduate from a master’s degree in Life Science or Pharmacy with some experience in Pharmacovigilance for example during studies, optional course or as a trainee
- Ability to communicate efficiently orally and in writing in local language and in English
- Structured and organized approach to work
- Ability to write medical
- Ability to use computerized applications and systems and especially Global PV Database
- Ability to liaise with the different functions ie Global Pharmacovigilance, Regulatory Affairs, Country Quality Assurance, businesses, Legal Affairs
What we can offer
- Sharing passion for Pharmacovigilance
- Great team -and work atmosphere
- Ability to influence and improve the overall processes with the team
- A company focusing on Inclusion and Diversity
- Being part of a digital journey and existing product innovations.
Baxter is committed to an Inclusive & Diverse environment for all employees to value and leverage differences in all aspects of our work to drive innovation and advance company culture where employees feel a sense of belonging and deep commitment to our mission. We are committed to attracting talent into Baxter that shares this commitment and to hiring the most qualified individual for the job, irrespective of disability, race, ethnicity, religion, gender or age.
#IND-NORD
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.
