Parexel

REGISTER YOUR INTEREST for the upcoming Senior Regulatory & Submissions Specialist positions. As soon as the role becomes available, we will promptly send you an email invitation to apply officially.

Currently, the position is hybrid office-based.

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 (ideally, 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.

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