Pharmacovigilance Scientists - Rixensart, België - GSK

GSK

Geverifieerd bedrijf

Rixensart, België

1 week geleden

Geplaatst door:

Sophie Dubois

beBee Recruiter

Beschrijving

Site Name:
UK - London - Brentford, Belgium-Rixensart, Belgium-Wavre, Canada - Ontario - Mississauga, Warsaw

Posted Date:
Feb

Pharmacovigilance Scientists - Associate Director/ Director/ Senior Director:
Positions in GSK Safety Evaluation and Risk Management (SERM) - Specialty Safety Business.

Exciting opportunities to make a significant impact on patients' lives

GSK is seeking talented, intellectually curious and experienced Pharmacovigilance Scientists who wish to join our Global Safety teams and contribute to the development and support of the next generation of transformational medicines and devices, that meet the needs of patients.

Our Safety Evaluation and Risk Management (SERM) teams are responsible for the assessment and interpretation of comprehensive safety information for GSK's medicines and devices in clinical development and on the market.

Our core capabilities include;

Safety signal detection, assessment and management;
Characterization, prevention and mitigation of safety risks,
Continuous assessment of the product benefitrisk profile;
Review, decisionmaking, leadership and crisis management for safety issues.

Our Safety Leads collaborate cross-functionally to develop and advance the safety strategy for marketed products and development assets in Respiratory medicines/devices, Allergy/immunoinflammatory and Dermatology, Neurosciences, Anti-infectives - anti-microbials/antivirals (ViiV Healthcare)/antimalarials, Urology, CV/Metabolic, Hepatology and many more.

This breadth creates the opportunity for you to learn and contribute across the entire product life cycle.

If you are
passionate about working with colleagues with world-class scientific expertise focused on delivering medicines and devices of significant value for patients and public health, we have Pharmacovigilance Scientist opportunities in the Specialty SERM Group**:

Bringing together more than 300 products, including best in class, first in class, growth and pipeline assets, our pharmacovigilance Specialty/General Medicines portfolio represents an incredible opportunity to impact the lives of 700+ million patients in the next 10 years. Many of the GSK heritage brands we manage are the leader in their therapy area or even the number one pharmaceutical brand on the market. We provide pharmacovigilance and comprehensive benefit-risk management for advanced Respiratory medicines and devices, Allergy/immunoinflammatory and Dermatology, Neurosciences, Anti-infectives including anti-microbials, antivirals (ViiV Healthcare) and antimalarials, Urology, CV/Metabolic, Hepatology and many more Product support ranges from R&D into Post-approval, Established & Generics.

We have exciting opportunities for you to join our team and be motivated by colleagues, engaged and energized by the science and inspired by the patients whose needs we strive to meet.

Come Join Our SERM Teams if You would like to:

Utilise your expertise as a PV Scientist to unite science, talent, and technology to deliver human health impact on a global scale.
Maintain your focus on the patient while delivering novel medications and devices that will truly transform the health of our communities.
Leverage continuous advances in data and technological capabilities to propel rich and robust safety insights.
Work with a global team that cultivates diversity, fosters inclusion, creates a respectful work environment, and encourages you to "Be You" and bring your best self to work.

_ As a SERM Scientific Associate __Director/ Director/ Senior Director you will have the following attributes:_**- Relevant Degree qualification. Higher level of education/qualification in life science discipline or relevant experience.

Advanced experience in the Pharmaceutical or Biotech industry working in Pharmacovigilance, Drug Safety, Medical Affairs, or a related field.
Significant pharmacovigilance experience relating to Safety Evaluation and Risk Management, encompassing both clinical development and postmarketing activities.
Knowledge/experience of international pharmacovigilance requirements (e.g., ICH, GVP modules, CIOMS initiatives) and drug development and approval processes.
Crossfunctional Matrix team leadership in large organizations.
Appropriate behavioural competencies.
Strong: Leadership Capability, Strategic Thinking, Business Acumen, Project Management, Communication Skills.
Ability to work across global sites.

Why Us?

GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organization where people can thrive.

Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.5 billion people by the end of 2030.

Our success absolutel