Regulatory Affairs Specialist- Belgian Dutch speaker- Remote
About this role
About the Role Regulatory Affairs Specialist who supports Belgian Dutch speaker in a remote role within Worldwide Clinical Trials' Regulatory Affairs team. You will coordinate regulatory submissions, ensure compliance with ICH GCP and EU-CTR requirements, and liaise with cross-functional teams to drive timely approvals across multiple regions. What You'll Do
- Liaise with SAR colleagues to plan, organize, compile, progress, track and submit regulatory submissions on a timely basis
- May act as a contact point for translation review of submissions documents such as application, synopsis, ICF, labels etc.
- Where required provide local QC of submission dossiers prior to dispatch
- Effectively communicate to the SAR Lead and relevant project team members the status and action plans concerning submissions
- Identify risks and generate mitigation strategies
Read the full description on TalentApply
Create a free account to see the complete job description, how well your CV matches this role, and apply in one click.
AI rewrites and formats your CV so it reads well and gets past screeners.
Get your match percentage for this exact role before you spend time applying.
Send a polished application in one click — no retyping the same details.
Follow every application in one place instead of digging through your inbox.
Free account · No card required
Your next opportunity starts here
Prepare, apply, track, interview and get hired — all from one platform, with AI in your corner.