Senior Regulatory Affairs Associate
3 weeks ago
We are looking for a **Senior **Regulatory Affairs Associate with working knowledge of Clinical Trial Applications (CTA) **to join our team in South Africa This role can be office based (Bloemfontein) or home based anywhere in South Africa.
As a Senior Regulatory Affairs Associate, you will ensure the timely performance of work within a project scope to the quality expectations of internal stakeholders and clients. You will bring your specialist knowledge of clinical trial submissions in Sub-Saharan countries. Aa s Senior Associate, under the general direction of a Project Lead and/or Technical SME, you will take responsibility for ensuring that client work is performed, and delivered on time, meeting the quality expectations of Parexel and our clients. You may take up a client facing role with support from line management.
**Key Deliverables in the role**:
- Manage the local submissions (as Local Regulatory Contact - LRC)
- Coordinate the regulatory submissions in all participating countries as Regulatory Lead.
- Regulatory submission of Clinical Trial in the region
- Participate in Regulatory Operations meetings, project team meetings, and maintain relationships with other departments, clients, and regulatory agencies as necessary.
- You may lead or be involved in local, regional, and/or global projects
- Guide and mentor junior team members
**Skills and Experience required for the role**:
- University degree in a science discipline
- Background in clinical trial management
- 3-5 years of Regulatory Affairs experience working with Clinical Trail Applications in South Africa
- Experience with clinical trial submissions in other Southern African Countries
- IT knowledge (Veeva Regulatory and Clinical Vaults - excel - VBA - powerBI)
- Customer-oriented and autonomous
- Fluency in English is a must along with the local language.
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