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- Support regulatory processes and ensure compliance with global regulations.
- Collaborate with cross-functional teams to gather and analyze data.
- Assist in the preparation of regulatory submissions.
- Monitor pharmacovigilance regulations and methodologies.
- Communicate effectively in English, both written and verbal, with a focus on scientific and medical terminology.
- Work with web-based applications and maintain a high level of computer proficiency.
- Prioritize tasks and maintain flexibility in a dynamic work environment.
Skills and Competencies:
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- Extensive knowledge of global regulatory processes.
- Strong attention to detail and ability to evaluate data.
- Good interpersonal, presentation, and communication skills.
- Service-oriented attitude and team player.
- Ability to build strong relationships and collaborate effectively.
- Commitment to high-quality results and continuous learning.
- Budgeting and cost-consciousness.
Why Join GSK?
GSK is a global biopharma company with a special purpose: to unite science, technology, and talent to get ahead of disease together. We focus on the science of the immune system and leverage new platform and data technologies across four core therapeutic areas: infectious diseases, HIV, respiratory/immunology, and oncology.
Our Values:
- Patient focus
- Transparency
- Respect
- Integrity
Our Expectations:
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- Courage
- Accountability
- Development
- Teamwork
Joining GSK means being part of an organization where people thrive, are inspired, encouraged, and challenged to be their best. We foster an inclusive environment where employees feel valued and can grow both personally and professionally.
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