At a Glance
- Tasks: Support the preparation of regulatory documents and collaborate with cross-functional teams.
- Company: Join a global healthcare leader with an exciting product pipeline.
- Benefits: Competitive salary, holidays, sick pay, pension, and hybrid work model.
- Other info: Gain hands-on experience and develop valuable skills in a supportive environment.
- Why this job: Kickstart your career in regulatory affairs and make a real impact on patient lives.
- Qualifications: Recent graduate with a passion for science and strong communication skills.
The predicted salary is between 31050 - 31050 £ per year.
An excellent opportunity for a talented graduate to start a career in regulatory affairs with a global healthcare leader, our client has one of the most exciting product pipelines in the industry today. Our mission is to improve patients' lives by providing customers with innovative science and differentiated healthcare solutions delivered by diverse and engaged talent with integrity, passion and focus on performance. Creativity and diversity are encouraged, impact is recognised, success is celebrated, and people feel valued and listened to.
The successful candidate will gain hands-on experience supporting the preparation of regulatory documents used throughout the drug development process and for submission to health authorities worldwide. Working within a global cross-functional environment, you will collaborate with colleagues from Regulatory Affairs, Clinical Development, Clinical Operations, Statistics and Drug Safety while developing valuable scientific communication and regulatory writing skills.
Your responsibilities will include, but are not limited to:
- Support the preparation and review of regulatory documents for submission to health authorities.
- Develop high-quality regulatory documents using approved templates, style guides and regulatory writing best practices.
- Collaborate with colleagues across Statistics, Clinical Operations, Clinical Development, Drug Safety and Regulatory Affairs to support the development of regulatory document content.
- Contribute to the planning and presentation of scientific and clinical data within regulatory documents.
- Support regulatory writing project plans and timelines to ensure deliverables are produced on time.
- Participate in cross-functional project teams and contribute towards achieving key project milestones.
- Learn and apply relevant regulatory requirements, company standards and industry best practices.
- Develop proficiency in regulatory writing technologies, document management systems and AI-enabled tools.
- Support continuous improvement initiatives and the sharing of best practices within the Regulatory Writing team.
Graduate Regulatory Writer employer: SRG
As a Senior Clinical Trial Manager at our company, you will thrive in a dynamic and collaborative work environment that prioritises innovation and employee development. We offer competitive benefits, a strong focus on professional growth, and the opportunity to work alongside industry leaders in a location renowned for its commitment to advancing clinical research. Join us to make a meaningful impact in the field of clinical trials while enjoying a supportive culture that values your contributions.
