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Pharmacovigilance Scientists

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Pharmacovigilance Scientists

GlaxoSmithKline Plc

Brentford, SD, USA Salary : $ 89,499 per year Apply Now
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Job Type: Full Time

Key Skills:

training Internship - <p>if You Make Hearts Beat Faster, Your Own Has To Be In The Right Place. Key Skills

  • Pharmacovigilance||Drug Development||Epidemiology||Literature||Pre-clinical Studies||BSN||Clinical Development||Excel Pivot||Microsoft Word||Pharmacoepidemiology

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

Posted Date:Mar 14 2023

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 benefit-risk profile;

  • Review, decision-making, 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 arepassionate 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 theSpecialty 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 AssociateDirector/ 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 post-marketing activities.

  • Knowledge/experience of international pharmacovigilance requirements (e.g., ICH, GVP modules, CIOMS initiatives) and drug development and approval processes.

  • Cross-functional 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.

As an Equal Opportunity Employer, we are open to all talent. In the US, we also adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to neurodiversity, race/ethnicity, colour, national origin, religion, gender, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class*(*US only).

We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on Ukdiversity.recruitment@gsk.com or 0808 234 4391. Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels

As you apply, we will ask you to share some personal information which is entirely voluntary. We want to have an opportunity to consider a diverse pool of qualified candidates and this information will assist us in meeting that objective and in understanding how well we are doing against our inclusion and diversity ambitions. We would really appreciate it if you could take a few moments to complete it. Rest assured, Hiring Managers do not have access to this information and we will treat your information confidentially.

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