Job Title: Regulatory Affairs CTA, CTR Manager/Consultant (Inside IR35)
Job Type: 12-month contract
Location: Berkshire, UK – Hybrid
Pay Rate: £65-75 per hour (PAYE)
We are partnered with a leading Pharmaceutical organization who are looking for an experienced Regulatory Consultant to join on a 12-month contract basis. You will work as a Regulatory EU CTR SME and support several EU CTR submissions.
As a Regulatory Affairs Professional, you will assume a crucial role in providing leadership and expertise in all regulatory and submission-related aspects of clinical trials. You will serve as the main point of contact and be responsible for delivering submission-specific milestones while offering guidance on submission strategies. Additionally, you will actively participate in EU-CTR consulting and contribute to the operational implementation aspects of the EU-CTR directive, ensuring effective collaboration between departments. Your role may also involve serving as a Clinical Trial Submission Coordinator/Lead, overseeing complex large clinical trial submissions.
Responsibilities:
• Lead/support all CTR initial submissions, transitions, amendments, and re-submissions
• Prepare all CTR-related documentation and be responsible for uploading this to the CTIS portal
• Work as an SME for the CTIS portal advising on how to use this system
• Participate in EU-CTR consulting and contribute to...