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Cta regulatory lead – clinical trial submissions (remote sa)

Company

Parexel International

Location

South-Africa, South-Africa

Type

Full-time

Parexel International is seeking an experienced Senior Regulatory Affairs Professional in South Africa. This position can be office-based in Bloemfontein or home-based anywhere in South Africa. The successful candidate will manage submissions for Clinical Trials and act as a Project Lead, ensuring all quality expectations are met.

The ideal candidate will have a science degree, regulatory affairs experience in South Africa, and strong problem-solving skills. Candidates should also be fluent in English and have knowledge of regulatory submissions across Southern Africa. #J-18808-Ljbffr

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