Remote Medical Writer

Placements24; Noord-Kaap; Hybrid; ZAR 600,000 - 900,000; Full time

Benefits offered by this job

Home office stipend

Health benefits

Professional development

Job summary

Placements24 is seeking a highly skilled Medical Writer for a fully remote role. You will craft clinical study reports, regulatory submissions, and scientific publications that meet stringent quality and regulatory standards for a global pharmaceutical company.

Responsibilities include authoring and reviewing regulatory documents, collaborating with experts, and managing timelines in a distributed team environment.

Qualifications

• Experience writing complex scientific and regulatory documents.
• Strong command of English grammar, style, and terminology.
• Ability to manage multiple projects remotely and meet timelines.

Responsibilities

• Author, edit, and review medical and regulatory documents (protocols, brochures, CSRs, submissions).
• Ensure materials are scientifically accurate and compliant with style guides and regulations.
• Collaborate with medical experts and regulatory professionals to gather information.

Skills

Medical writing

Regulatory documentation

Regulatory submissions

Attention to detail

Remote collaboration

Education

Bachelor’s or Master’s in life sciences

Job description

About the Role

Our client is seeking a talented and highly skilled Medical Writer for a fully remote position. This role is essential for crafting clear, accurate, and scientifically sound medical documentation to support pharmaceutical development and regulatory submissions. You will work on a variety of documents, including clinical study reports, regulatory submission documents, and scientific publications, ensuring they meet stringent quality and compliance standards. This is an excellent opportunity for a professional writer to leverage their expertise in a flexible, remote work environment, contributing to the communication of vital medical and scientific information for a global pharmaceutical company, collaborating effectively with dispersed teams.

Key Responsibilities

• Author, edit, and review a range of medical and regulatory documents, including clinical protocols, investigator brochures, CSRs, and submission dossiers.
• Ensure all written materials are scientifically accurate, clearly written, and adhere to relevant style guides and regulatory requirements.
• Collaborate closely with medical experts, researchers, and regulatory affairs professionals to gather information and ensure the quality of documentation.
• Manage document development timelines and coordinate contributions from multiple authors and reviewers.
• Maintain up-to-date knowledge of pharmaceutical regulations, guidelines, and best practices for medical writing.

Requirements

• Bachelor's or Master's degree in a life science, pharmacy, or a related field.
• Minimum of 4 years of experience as a Medical Writer in the pharmaceutical or biotechnology industry.
• Proven ability to write complex scientific and regulatory documents accurately and efficiently.
• Excellent command of English grammar, style, and scientific terminology.
• Strong organizational skills and the ability to manage multiple projects simultaneously in a remote setting.

Benefits

• Competitive annual salary and performance-based incentives.
• Comprehensive health and wellness benefits package.
• Home office setup stipend and ongoing professional development opportunities.
• Flexible work schedule and the ability to work from anywhere.
• A dynamic and collaborative remote work environment focused on delivering high-quality medical communications.