At a Glance
- Tasks: Coordinate regulatory submissions and ensure compliance with global strategies.
- Company: Join CCS Global, a leader in clinical research and regulatory affairs.
- Benefits: Competitive salary, flexible working hours, and opportunities for professional growth.
- Other info: Dynamic team environment with a focus on innovation and collaboration.
- Why this job: Make a difference in global health by supporting vital clinical studies.
- Qualifications: 2+ years in regulatory affairs and strong communication skills required.
The predicted salary is between 63000 - 77000 £ per year.
CCS Global is seeking a Country Approval Specialist in the United Kingdom to support local regulatory submissions aligned with global strategy.
You will coordinate submissions to Mo H, EC and national applications, and collaborate with sites, CROs and Clinical Operations to ensure timely, compliant e TMF records and activation.
The role requires strong attention to detail, excellent communication, and knowledge of FDA/ICH-GCP guidelines, with 2+ years of relevant experience in regulatory affairs.
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Global Study Start-Up Specialist employer: CCS-Global
CCS Global is an exceptional employer, offering Clinical Research Associates the chance to work with a leading organisation dedicated to advancing clinical research and improving patient outcomes. With a strong emphasis on career development, comprehensive training, and broad therapeutic exposure, employees can expect a supportive work culture that prioritises quality and innovation in clinical trials across the UK. Join us to be part of a forward-thinking team that values your expertise and fosters meaningful growth opportunities.
