Full job descriptionJob 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:
*Lead a team of Content Strategists and cross-functional teams in creating and executing content strategies for global regulatory submissions.
*Develop and maintain timelines for document production and review, ensuring alignment with project milestones.
*Review documents for clarity, scientific rigour, and consistency, resolving issues with cross-functional contributors.
*Actively participate in functional and cross-functional teams, contributing to best practises and continuous improvement initiatives.
*Partner with key stakeholders to drive initiatives that influence our technical, business, and healthcare landscape.
*Stay updated on regulatory, scientific, and medical topics relevant to drug development.
Who You Are:
*A degree in Life Sciences or equivalent, with experience in the pharmaceutical/biotechnology industry.
*Proven experience leading cross-functional teams and delivering projects independently.
*Familiarity with global drug and device development processes, regulations, and guidelines (GxP, GCP, ICH, ISO, MDR/IVDR).
*Expertise in clinical and safety regulatory documentation throughout the product lifecycle.
*Strong analytical skills with the ability to synthesise complex data and concepts.
*Excellent communication and interpersonal skills for building trust and fostering collaboration across diverse teams.
*Proficient in Microsoft Office Suite, G Suite, Adobe Acrobat, and Veeva Vault; detail-oriented with a creative mindset.
*Fluent in English (verbal and written).
Contract Details:
*Contract Type: Temporary (12 months) Outside IR35
*Hourly Rate: £60.00 - £75.00 UMB
*Working Style: Fully remote or hybrid options available.
Why Join Us?
*Play a crucial role in advancing healthcare and improving patient outcomes.
*Collaborate with talented professionals in a dynamic and innovative environment.
*Enjoy a competitive rate and flexible working arrangements.
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.