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Open nowPosted 14 days ago

NON CLINICAL SAFETY TRAINEE

almirall53 open roles

Where
SANT FELIU DE LLOBREGAT
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Your applicationOpen nowNON CLINICAL SAFETY TRAINEEalmirall · SANT FELIU DE LLOBREGAT

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

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The clock on this job

Early applications get read.

12.7% of postings close within 7 days. Measured by our own scanner across the market. almirall postings stay open a median of 14 days.

Share of postings closed within
  1. 2.2%1 day
  2. 4.5%3 days
  3. 12.7%7 days
  4. 20.4%14 days
  5. 35.6%30 days
  6. 58.7%60 days
This job: posted 14 days ago

almirall median: 14 days open

The posting

We’re building the future of medical dermatology by focusing on unmet patient needs and giving people the space to think independently, take ownership and make an impact that matters.

Our purpose is simple: to transform patients’ lives by addressing real needs. We work with care, act with courage, keep things simple and focus our innovation where it makes a difference.

Recognised as a Top Employer in Spain since 2008 and in Germany since 2025, we continue to invest in an environment where people can grow and move forward.

If you care differently, you belong here.

Mission

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.

Functions and responsibilities

Scientific & Safety assessment support

  • 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.

Outsourcing & External studies

  • 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.

Study documentation & Archiving

  • 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.

Operational & Digital support

  • 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.

Learning & Development

  • 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.

Education

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

Specific expertise

  • Fluent English, written and spoken.
  • 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.

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.

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