Remote Senior Medical Writer – Oncology & Regulatory Lead

Mms Holdings Inc.; Durban; Remote; ZAR 800 000 - 1 200 000; Full time

Job summary

A leading clinical research organization in South Africa is seeking a Senior Medical Writer. In this home-based role, you will manage writing regulatory documents, mentor team members, and contribute to clinical study protocols. The ideal candidate has over 5 years of experience in regulatory and clinical writing, exceptional writing skills, and a strong understanding of oncology. Join a supportive team where your contributions matter.

Qualifications

• At least 3 years of previous experience in the pharmaceutical industry.
• 5 years of regulatory writing and clinical medical writing experience.
• Substantial clinical study protocol experience, as lead author.

Responsibilities

• Communicate competitively for projects.
• Manage production of interpretive guides.
• Mentor medical writers involved in the writing process.

Skills

Regulatory writing

Oncology experience

Exceptional writing skills

Organizational skills

Project management

Education

Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline

Tools

MS Word

Excel

PowerPoint

Job description

A leading clinical research organization in South Africa is seeking a Senior Medical Writer. In this home-based role, you will manage writing regulatory documents, mentor team members, and contribute to clinical study protocols. The ideal candidate has over 5 years of experience in regulatory and clinical writing, exceptional writing skills, and a strong understanding of oncology. Join a supportive team where your contributions matter.