Senior Regulatory Specialist (FSP) REGISTER YOUR INTEREST

Accountable for performance and compliance with assigned protocols in a country in compliance with ICH/GCP and country regulations, Client policies and procedures, quality standards, and adverse event reporting requirements internally and externally.

Experience required to be a fit for this role:

· Mandatory - experience in EC and RA submission (must be familiar with XML completion) – including initial submission and protocol amendments submission.

· Experience in Independently preparing submissions (CTC supports with

document collection) to both EC and RA.

· Experience in ICF preparation using templates.

· Skilled knowledge of the local regulatory environment, submissions, and approval processes, and understanding of how these impact study start-ups.

· Experience in IMP supplies management at the local level (vendors providing background meds, the standard of care, etc.)

· Experience in validation of translated documents.

We offer exceptional financial rewards, training, and development. Expect exciting professional challenges but with a healthy work/life balance. We value your welfare just as highly as that of our patients.