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Title
Text copied to clipboard!Medical Writer
Description
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We are looking for a Medical Writer to join our dynamic team. As a Medical Writer, you will be responsible for creating high-quality, scientifically accurate documents that communicate complex medical information clearly and effectively. Your work will support clinical research, regulatory submissions, medical education, and marketing initiatives. You will collaborate with subject matter experts, researchers, clinicians, and regulatory professionals to ensure that all documents meet the highest standards of accuracy, clarity, and compliance. Key tasks include writing clinical study protocols, investigator brochures, informed consent forms, clinical study reports, manuscripts for peer-reviewed journals, abstracts, posters, and slide presentations. You will also be involved in preparing regulatory documents such as INDs, NDAs, and CTDs, as well as educational and promotional materials for healthcare professionals and patients. Attention to detail, strong organizational skills, and the ability to manage multiple projects simultaneously are essential. You must be able to interpret and synthesize complex scientific data, adhere to strict deadlines, and maintain compliance with industry guidelines and regulations. The ideal candidate will have a background in life sciences, excellent written and verbal communication skills, and experience in medical or scientific writing. Familiarity with regulatory requirements, publication standards, and medical terminology is highly desirable. You will play a critical role in ensuring that scientific and medical information is communicated accurately, ethically, and effectively to a variety of audiences, including regulatory agencies, healthcare professionals, and the general public.
Responsibilities
Text copied to clipboard!- Write and edit clinical study protocols and reports
- Prepare regulatory documents for submissions
- Develop manuscripts, abstracts, and posters for publication
- Collaborate with subject matter experts and project teams
- Ensure accuracy and clarity of scientific content
- Adhere to regulatory and publication guidelines
- Manage multiple writing projects and meet deadlines
- Review and revise documents based on feedback
- Maintain up-to-date knowledge of medical literature
- Support the development of educational and promotional materials
Requirements
Text copied to clipboard!- Bachelor’s or Master’s degree in life sciences or related field
- Proven experience in medical or scientific writing
- Excellent written and verbal communication skills
- Strong attention to detail and organizational skills
- Ability to interpret and synthesize complex scientific data
- Familiarity with regulatory and publication standards
- Proficiency in Microsoft Office and document management tools
- Ability to work independently and as part of a team
- Experience managing multiple projects simultaneously
- Knowledge of medical terminology and clinical research processes
Potential interview questions
Text copied to clipboard!- What is your experience with medical or scientific writing?
- Can you provide examples of documents you have written?
- How do you ensure accuracy and clarity in your writing?
- Describe your experience with regulatory submissions.
- How do you manage tight deadlines and multiple projects?
- What is your familiarity with medical terminology?
- Have you worked with cross-functional teams before?
- What tools or software do you use for writing and editing?
- How do you stay updated with medical literature?
- Describe a challenging writing project and how you handled it.
