At a Glance
- Tasks: Lead post-approval CMC activities for vaccines and develop submission strategies.
- Company: Join Parexel International, a leader in regulatory affairs with a global impact.
- Benefits: Flexible remote work options, competitive salary, and opportunities for professional growth.
- Other info: Collaborative environment with diverse teams across Europe.
- Why this job: Make a difference in global health by working on innovative vaccine projects.
- Qualifications: Experience in regulatory affairs and fluency in English required.
The predicted salary is between 60000 - 80000 £ per year.
Parexel International is seeking an experienced Regulatory Affairs Consultant to join our team on a client-dedicated project.
The role can be office or home based in various European locations.
You will lead post-approval CMC activities for vaccines or biological products, develop submission strategies, assess change controls, and coordinate with manufacturing, QA, and other regulatory teams to ensure worldwide submissions.
Fluency in English is required.
#J-18808-Ljbffr
Remote Post-Approval CMC Regulatory Consultant (Vaccines) employer: Parexel International
At Parexel International, we pride ourselves on being an exceptional employer, offering a collaborative and innovative work culture that empowers our employees to excel in their roles. With a strong focus on professional development, we provide ample opportunities for growth and advancement within the clinical research field, particularly in the UK and Germany, where our teams are dedicated to making a meaningful impact on patient care through cutting-edge clinical trials.
