Safety Scientist II/III – Clinical Drug Safety
Thermo Fisher Scientific · Afrique du Sud
Description du poste
About the role
Thermo Fisher Scientific is seeking a Safety Scientist II/III to join its EMEA drug safety team. You will play a pivotal role in managing the safety profile of new medicines throughout clinical development, ensuring high‑quality signal detection, case processing, and regulatory reporting.
Key responsibilities
- Plan, coordinate and deliver signal detection and product safety activities across low to ultra‑high complexity products.
- Create and contribute to safety assessments, quality reviews, and regulatory submissions under supervision.
- Lead small pharmacovigilance (FSP) projects and support bid defence and proposal development.
- Mentor junior colleagues and contribute to the development of processes, tools, and systems.
- Interact with project teams, clients, and multiple internal systems while adhering to company policies and regulatory requirements.
Required profile
- Experience in clinical drug safety, pharmacovigilance, or related scientific fields.
- Ability to work independently on complex safety tasks and provide guidance to less‑experienced team members.
- Strong analytical mindset with attention to detail and commitment to data quality.
- Effective communication skills for client interaction and internal collaboration.
Required skills
- Signal detection methodologies
- Product safety assessment
- Regulatory reporting processes
- Quality review techniques
What we offer
- Career advancement opportunities within a global scientific organization.
- Award‑winning training programs focused on health and wellbeing.
- Collaborative, mission‑driven work environment.
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Thermo Fisher Scientific
Afrique du Sud
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