Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.
This role combines scientific expertise with innovation, shaping how safety data is assessed, interpreted, and communicated across a global environment. Ideal for a strategic thinker passionate about advancing signal detection, safety writing, and AI-enabled transformation.
Main Responsibilities:
- Drive initiatives to enhance Benefit–Risk Assessment & Management (BRAM) practices, tools, and processes
- Lead and deliver capability-building and transformation projects, from planning to implementation
- Manage project timelines, milestones, and stakeholder communication
- Oversee daily activities across signal detection and safety writing workflows (processes, tools, data, documentation)
- Support continuous improvement of BRAM infrastructure and ensure regulatory compliance
- Implement process and SOP updates within safety and signal detection systems
- Collaborate with IT to advance digital transformation (automation, workflow optimisation, AI integration)
- Apply strong expertise in signal detection and safety writing to ensure high-quality outputs
Requirements
- Bachelor’s degree in Life Sciences or related field
- 10+ years of biopharmaceutical experience, with strong expertise in signal detection, safety writing, and risk management
- Solid understanding of global GCP/GVP regulations and industry standards
- Proven experience in leading change and driving transformation initiatives
- Strong communication and presentation skills in English
- Ability to work autonomously, manage multiple priorities, and collaborate effectively in a matrix environment
- Demonstrates adaptability, resilience, and a results-driven mindset
Benefits
Why Join Us?
At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.
Here’s what makes us unique—
We are a young, ambitious health company representing 900 Excelyates, driven to become Europe’s leading mid-size CRO with the best employee experience. Our one-stop provider service model—offering full-service, functional service provider, and consulting—enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient’s journey.
Excelling with care means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.
Skills Required
- Bachelor's degree in Life Sciences or related field
- 10+ years of biopharmaceutical experience
- Strong expertise in signal detection, safety writing, and risk management
- Solid understanding of global GCP/GVP regulations and industry standards
- Proven experience in leading change and driving transformation initiatives
- Strong communication and presentation skills in English
- Ability to work autonomously, manage multiple priorities, and collaborate effectively
What We Do
Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of Full-service CRO, FSP, and Resourcing solutions guided by compassion, care, and excellence. Founded in 2014 and headquartered in Paris, France, and operating in 28 countries across Europe, USA and India, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas, with speciality focus on Oncology & Hematology, Rare Disease & Pediatrics, Infectious Disease, Inflammation & Immunotherapy, Pain Treatment & CNS, and Late Phase & RWE.
