Regulatory Medical Writer — Remote, Flexible Hours, Growth

Placements24; Paarl; Hybrid; ZAR 480,000 - 600,000; Full time

Benefits offered by this job

Competitive salary

Medical coverage

Paid time off

Flexible hours

Remote-friendly work

Job summary

Placements24 seeks a skilled Medical Writer to produce regulatory documents for pharmaceutical products from Paarl. You will author, edit, and review clinical study reports, regulatory submission documents, and CTD modules with clarity and scientific rigor.

The role requires a life sciences degree and a minimum of 3 years’ regulatory writing experience, with the ability to translate complex data into concise text while meeting tight deadlines in a collaborative, remote-friendly environment.

Qualifications

• Bachelor's degree in a scientific discipline (Life Sciences, Pharmacy, Medicine).
• Minimum of 3 years of experience as a Medical Writer in pharmaceutical/biotech with focus on regulatory documentation.
• Proven ability to write clear, concise, scientifically accurate documents for diverse audiences.
• Strong understanding of clinical trial processes, pharmaceutical development, and regulatory requirements.
• Proficiency in standard office software and document management systems.
• Excellent organizational skills and ability to manage multiple projects under tight deadlines.

Responsibilities

• Author, edit, and finalize regulatory documents such as CSRs and CTD modules.
• Ensure documents are scientifically accurate and adhere to guidelines.
• Collaborate with cross-functional teams to gather information for submissions.
• Review and revise documents based on stakeholder feedback.
• Maintain knowledge of regulatory guidelines and best practices.

Skills

Regulatory writing

Scientific writing

Attention to detail

Education

Bachelor's degree in Life Sciences/Pharmacy/Medicine

Job description

Placements24 seeks a skilled Medical Writer to produce regulatory documents for pharmaceutical products from Paarl. You will author, edit, and review clinical study reports, regulatory submission documents, and CTD modules with clarity and scientific rigor.

The role requires a life sciences degree and a minimum of 3 years’ regulatory writing experience, with the ability to translate complex data into concise text while meeting tight deadlines in a collaborative, remote-friendly environment.