Clinical Protocol Architect for Global Trials

Ajpersonnel; Durban; On-site; ZAR 500 000 - 700 000; Full time

Job summary

A leading clinical research organization in Durban seeks an experienced clinical trial professional to develop and maintain Standard Operating Procedures. The ideal candidate will have a Master's degree in a relevant field, with a PhD being advantageous. Responsibilities include managing clinical trial documentation, leading protocol meetings, and ensuring compliance with regulatory standards. Applicants must demonstrate previous clinical trial experience and a strong publication record. This is a 2-year fixed-term contract, renewable, with applications closing on 10 October 2025.

Qualifications

• Masters Degree in a relevant field.
• PhD is advantageous.
• Experience in clinical trials required.
• Knowledge of trial protocol and case report form development.
• Experience in producing annual drug safety reports.

Responsibilities

• Develop and maintain Standard Operating Procedures.
• Draft Clinical Study Report at the end of trials.
• Lead protocol writing meetings.
• Update Investigator's Brochure with new data.

Skills

Clinical trial protocol development

Medical writing

Data analysis

Project management

Publication in peer-reviewed journals

Education

Masters Degree in Science, Medicine, Immunology, Microbiology, Public Health

PhD

Tools

MS Office

MS Project

Job description

A leading clinical research organization in Durban seeks an experienced clinical trial professional to develop and maintain Standard Operating Procedures. The ideal candidate will have a Master's degree in a relevant field, with a PhD being advantageous. Responsibilities include managing clinical trial documentation, leading protocol meetings, and ensuring compliance with regulatory standards. Applicants must demonstrate previous clinical trial experience and a strong publication record. This is a 2-year fixed-term contract, renewable, with applications closing on 10 October 2025.