Job Title: Regulatory Data and Content Professional (Senior Medical Writer)
Are you passionate about advancing healthcare and making a real impact in the pharmaceutical and biotechnology sectors? Join our innovative organisation and help shape the future of medicine!
About Us:
We are a bold and flexible regulatory organisation committed to driving science forward, ensuring access to healthcare for everyone. Our Pharma Development Regulatory (PDR) team is at the forefront of data interpretation and content strategy, dedicated to submitting high-quality documents to global health authorities.
The Opportunity:
As a Regulatory Data and Content Professional, you will lead and manage data interpretation and medical writing from initiation to approval, contributing to the development of Roche product permits and licences.
Key Responsibilities:
Who You Are:
Contract Details:
Why Join Us?
If you're ready to make a difference and drive outcomes in global regulatory projects, we want to hear from you! Apply now to join our team and help us create a healthier future for all.
Note: Relocation benefits are not available for this position.
Adecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.
We use generative AI tools to support our candidate screening process. This helps us ensure a fair, consistent, and efficient experience for all applicants. Rest assured, all final decisions are made by our hiring team, and your application will be reviewed with care and attention.
