Medical Writer - Remote

Placements24; Soweto; Hybrid; ZAR 600,000 - 900,000; Full time

Benefits offered by this job

Fully remote work

Competitive compensation

Professional development

Job summary

Placements24 is seeking a talented Medical Writer to join their global team remotely. You will create clear, scientifically sound documents for regulators, healthcare professionals, and patients, translating complex clinical data into high-quality written content.

The role requires an advanced degree in life sciences, at least 5 years in medical writing within pharma/biotech, and exceptional English; you will collaborate with SMEs, manage multiple projects, and ensure compliance with regulatory

Qualifications

• Advanced degree in life sciences or related field.
• Minimum of 5 years of experience as a Medical Writer in pharma/biotech.
• Proven ability to write clear, concise, scientifically accurate documents.
• Thorough understanding of clinical trial processes and regulatory submission requirements.
• Excellent command of English grammar, style, and terminology.
• Strong organizational skills to manage projects remotely.

Responsibilities

• Write, edit, and review CSRs, protocols, IBs, and submission dossiers.
• Develop patient-facing materials summarizing trial results.
• Ensure documents are scientifically accurate and regulatory compliant.
• Collaborate with clinicians, scientists, and regulatory specialists.
• Manage multiple writing projects with strict deadlines.
• Stay updated on industry best practices and guidelines.

Skills

Scientific writing

Regulatory writing

English proficiency

Remote work

Education

Master's or PhD in life sciences

PhD in life sciences

Job description

About the Role

Our client is seeking a talented and experienced Medical Writer to join their global team, working entirely remotely. This role is responsible for creating clear, accurate, and scientifically sound documents for a variety of audiences, including regulatory bodies, healthcare professionals, and patients. You will translate complex scientific and clinical data into high-quality written content, ensuring consistency and adherence to relevant guidelines. This is an excellent opportunity for a skilled writer to contribute to impactful medical communications from a remote setting, working collaboratively with cross-functional teams to disseminate critical information about pharmaceutical products.

Key Responsibilities

• Write, edit, and review various medical documents, such as clinical study reports (CSRs), protocols, Investigator's Brochures (IBs), and submission dossiers.
• Develop patient-facing materials, including summaries of clinical trial results and educational content.
• Ensure all medical documentation is scientifically accurate, compliant with regulatory requirements, and meets internal quality standards.
• Collaborate with subject matter experts (SMEs) including clinicians, scientists, and regulatory specialists.
• Manage multiple writing projects simultaneously, adhering to strict deadlines.
• Stay updated on industry best practices and regulatory guidelines for medical writing.

Requirements

• Advanced degree (e.g., Master's, PhD) in a life science, medical, or related field.
• Minimum of 5 years of experience as a Medical Writer in the pharmaceutical or biotechnology industry.
• Proven ability to write clear, concise, and scientifically accurate documents.
• Thorough understanding of clinical trial processes and regulatory submission requirements.
• Excellent command of English grammar, style, and scientific terminology.
• Strong organizational skills and ability to manage projects independently in a remote setting.

Benefits

• Competitive annual salary based on experience and qualifications.
• Fully remote work opportunity, providing ultimate flexibility.
• Comprehensive medical, dental, and vision insurance coverage.
• Generous paid time off and professional development allowances.
• Opportunity to work on diverse and critical medical communication projects.