At a Glance
- Tasks: Coordinate global clinical trial applications and manage submission timelines.
- Company: Join Simbec-Orion, a flexible CRO dedicated to improving patient outcomes.
- Benefits: Enjoy a supportive work environment with opportunities for professional growth.
- Other info: Flexible working arrangements and a focus on team collaboration.
- Why this job: Make a real difference in healthcare by ensuring compliance and mentoring others.
- Qualifications: Extensive experience in regulatory submissions and strong ICH-GCP knowledge.
The predicted salary is between 63000 - 77000 £ per year.
Simbec-Orion is seeking a Senior Regulatory Affairs Associate to coordinate global clinical trial applications for medical products and devices, ensuring alignment with ICH and regulatory guidelines.
You will manage submission timelines and keep stakeholders informed across the project.
The role requires extensive experience in regulatory submissions, strong ICH-GCP knowledge, and the ability to mentor junior staff.
Join a flexible CRO focused on improving patient outcomes.
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Senior Regulatory Lead - Global Clinical Trials employer: Meeveem Limited
Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.
