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Regulatory Affairs Associate
Found in: Talent ZA C2 - 4 hours ago
Parexel Bloemfontein, South Africa Full timeWhen our values align, there's no limit to what we can achieve. · We are looking for an experienced Regulatory Affairs Professional with working knowledge of Clinical Trail Applications (CTA) to join our team in South Africa This role can be office based (Bloemfontein) or home ...
Senior Regulatory Specialist - Bloemfontein, South Africa - Parexel
Description
When our values align, there's no limit to what we can achieve.
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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