We are looking for an experienced Regulatory Affairs Professional 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 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 may act as a Project Lead or Work Stream Lead and in this role you will assure the work of the entire team or work stream is delivered on time and that it meets client’s quality expectations. You will succeed in this role because will bring your strong technical skills and may be developing specialist knowledge of a particular subject and/ or market.

Key Deliverables in the role:

Manage the local submissions (as Local Regulatory Contact - LRC) but should also be able to coordinate the regulatory submissions in all participating countries as Regulatory Lead.

Regulatory submission of Clinical Trial in South Africa

​​​Participate in Regulatory Operations meetings, project team meetings, and maintain relationships with other departments, clients, and regulatory agencies as necessary.

You may be involved in local, regional, and/or global projects

Skills and Experience required for the role:

University degree in a science discipline

Background in clinical trial management

1-2 years of Regulatory Affairs experience working with Clinical Trail Applications in South Africa

Experience with clinical trial submissions in other Southern African Countries - preferred

Good level of knowledge of the CTA business in addition, an expertise/skill in cross-functional project management and planning, process optimization

IT knowledge (Veeva Regulatory and Clinical Vaults - excel – VBA – powerBI)

Solid analysis and synthesis capability; Solution-oriented and problem-solving skills.

Customer-oriented and autonomous

Fluency in English is a must along with the local language.