Non-Clinical Safety Trainee

• Good knowledge of Microsoft Office tools (Excel, PowerPoint, Word).
• Strong analytical and organizational skills.
• Interest in toxicology, drug development and scientific data analysis.
• Curiosity for digital and AI-enabled solutions.
• Strong attention to detail and willingness to learn.

• Bachelor's degree in Health Sciences, Pharmacy, Biotechnology, Biomedical Sciences or related disciplines.
• Currently pursuing a Master's degree related to the pharmaceutical industry.

• Fluent English, written and spoken.

To gain practical experience in Non-Clinical Safety while supporting scientific, operational and digital activities that contribute to the development of safe and effective medicines.

The trainee will work closely with experienced toxicologists and will be exposed to multiple aspects of drug discovery and development, including safety assessments, outsourced studies, data management and process improvement initiatives.

The position is focused on scientific, operational and digital support activities and does not involve laboratory-based experimental work.

• Learn key principles of non-clinical safety assessment, toxicology and regulatory sciences.
• Gain exposure to the role of Non-Clinical Safety across drug discovery and development.
• Participate in team meetings, scientific discussions, webinars and training activities.

Join the Non-Clinical Safety team and gain exposure to scientific, operational and digital activities supporting the development of safe and effective medicines. The trainee will contribute to safety assessments, outsourced study management, data organization, digital initiatives and process improvement projects within pharmaceutical R&D.

• Support literature reviews, benchmarking activities and preliminary Target Safety Assessments (TSAs).
• Contribute to scientific evaluations related to target biology, safety risks and non-clinical data.
• Assist in gathering and organizing information from internal and external sources to support project discussions.
• Support management of outsourced non-clinical studies, including timelines, budgets, purchase orders and study documentation.
• Participate in interactions with CROs and contribute to study monitoring activities, follow-up of action items and study coordination.
• Assist in the review of quotations and comparison of external providers.
• Compile, organize and upload study results and documents to internal repositories and electronic document management systems.
• Support archiving activities and maintenance of study records.
• Contribute to maintaining traceability and documentation quality standards.
• Support maintenance of study trackers, timelines, budgets and key performance indicators.
• Assist in preparing meeting minutes and follow-up actions.
• Contribute to process improvement initiatives, including templates, SOPs and Working Instructions.
• Explore digital and AI-based solutions to improve data retrieval, summarization, visualization and operational efficiency.
• Support the implementation and adoption of new digital tools and workflows to improve project tracking, collaboration and operational efficiency.