Remote Medical Writer

Placements24; Gqeberha; Hybrid; ZAR 700.000 - 1.000.000; Vollzeit

Benefits dieser Stelle

Remote work setup

Competitive salary

Full benefits

Professional growth

Flexible schedule

Zusammenfassung

Placements24 in Port Elizabeth is seeking an experienced Remote Medical Writer to join our expanding communications team.

You will translate complex clinical data into regulatory submissions, manuscripts, and abstracts for audiences worldwide, with a focus on accuracy, clarity, and compliance.

This fully remote role offers a competitive salary, full benefits, and opportunities for professional growth in medical communications.

Qualifikationen

• Advanced degree in life sciences.
• Minimum 4 years' medical writing experience in pharma/biotech.
• Ability to write complex documents for diverse audiences.
• Strong knowledge of regulatory requirements and trial processes.

Aufgaben

• Author, edit, and review clinical study reports, regulatory submissions, manuscripts, and abstracts.
• Ensure scientific accuracy and clear communication aligned with project goals.
• Collaborate with medical experts, regulatory, and marketing teams to ensure content accuracy.
• Adhere to FDA/EMA guidelines and company SOPs.
• Manage multiple writing projects remotely with strict deadlines.

Kenntnisse

Medical writing

Regulatory knowledge

Clinical trial understanding

Remote work

Attention to detail

Ausbildung

Master's degree in life sciences

PhD in life sciences or related field

Jobbeschreibung

About the Role

Our client is actively seeking a talented and experienced Remote Medical Writer to join their expanding communications team, working entirely from their home office, serving clients globally from a base in Port Elizabeth . This role is critical in translating complex scientific and clinical data into clear, accurate, and compelling documents for various audiences, including healthcare professionals, regulatory agencies, and patients. You will be responsible for producing a range of high-quality medical and scientific documents, ensuring compliance with relevant guidelines and company standards. This position offers a fantastic opportunity for a skilled writer who thrives in a remote setting and is passionate about science communication.

Key Responsibilities

• Author, edit, and review a variety of medical documents, including clinical study reports (CSRs), regulatory submissions, manuscripts, and abstracts.
• Ensure all written materials are scientifically accurate, clear, concise, and meet the objectives of the project.
• Collaborate with cross-functional teams, including medical experts, regulatory affairs, and marketing, to gather information and ensure content accuracy.
• Adhere to relevant style guides, regulatory requirements (e.g., FDA, EMA), and company SOPs for document creation.
• Manage multiple writing projects simultaneously, ensuring timely delivery and high-quality output.
• Contribute to the development of publication plans and ensure compliance with journal and conference guidelines.

Requirements

• Advanced degree (Master's or Ph.D.) in a life science, medical field, or related discipline.
• Minimum of 4 years of experience as a Medical Writer in the pharmaceutical or biotechnology industry.
• Demonstrated ability to write complex scientific and clinical documents for diverse audiences.
• Excellent understanding of clinical trial processes, regulatory requirements, and scientific principles.
• Exceptional written and verbal communication skills, with meticulous attention to detail.
• Proven ability to work independently and manage projects effectively in a remote work environment.

Benefits

• Competitive annual salary package.
• Full remote work setup and technology support.
• Comprehensive health, dental, and vision insurance.
• Opportunities for professional growth and development in medical communications.
• A flexible work schedule and the chance to work on diverse and impactful projects.