Compliance Consultant

2 months ago


London, United Kingdom Clinical Professionals Limited Full time

Regulatory Affairs Consultant – CTA/EU-CTR
Job Type: Permanent
Regulatory Affairs Consultant – CTA/EU-CTR (freelancer)
6-12 month contract
Poland, Romania, Croatia, Czech Republic, Italy & UK (Fully Remote)
An exciting opportunity to work as a Regulatory EU CTR SME and support several clients with EU CTR submissions. We are currently seeking Regulatory Affairs Professionals on various levels with experience in Clinical Trial Applications (CTAs) under the EU-CTR directive.
Join the team or work on dedicated client projects as a Senior Regulatory Affairs Consultant, Regulatory Affairs Consultant, or Regulatory Affairs Senior Associate. This will be a temporary contract (6-12 months) with the opportunity to potentially go permanent after the contract completion. The role can be home, or office based in various European locations.
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. 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. Participate in EU-CTR consulting and contribute to its operational implementation
· Provide leadership and expertise in regulatory and submissions-related aspects of clinical trials
· University degree in a scientific discipline
· Experience in Regulatory Affairs
· Good level of knowledge of Clinical Trial Submissions on a local and regional level
· Fluency in English is a must (written and spoken), along with proficiency in the local language



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