Medical / Regulatory Writer
2 weeks ago
You must have a deep understanding of medical terminology, the ability to convey complex information in a way that is accessible to different audiences, and the capacity to work with healthcare professionals, researchers, and regulatory bodies to ensure that the content meets industry standards.
- Research and write high-quality medical content, including but not limited to articles, white papers, research papers, patient information leaflets, case studies, and product descriptions.
- Develop content for healthcare professionals, researchers, and patients, ensuring accuracy and clarity.
- Summarize and interpret clinical trial data, medical studies, and regulatory guidelines.
- Collaborate with medical professionals, subject matter experts, and editorial teams to ensure accuracy and alignment with client goals.
- Stay updated on medical research, healthcare advancements, and regulatory changes.
- Ensure all written materials meet client guidelines, including compliance with medical regulations and scientific accuracy.
- Edit and proofread content for grammar, style, and consistency, adhering to AMA or other relevant writing styles.
- Adapt content to suit different audiences, including specialists, patients, and regulatory authorities.
- Manage deadlines and revisions efficiently, maintaining high-quality standards across all projects.
- Bachelor's degree in a medical or life sciences field (e.g., Medicine, Nursing, Pharmacology, Biology, etc.); advanced degrees (MD, PhD, MPH) preferred.
- Proven experience as a medical writer or editor, with a portfolio demonstrating relevant work in healthcare, pharmaceuticals, biotechnology, or clinical research.
- Strong understanding of medical terminology, healthcare concepts, and scientific methodology.
- Excellent written communication skills, with the ability to translate complex medical information into clear, understandable content.
- Familiarity with regulatory requirements (FDA, EMA, etc.) and writing clinical trial documentation (clinical study reports, protocols, informed consent forms).
- Proficiency in referencing and using medical literature databases (e.g., li>
- Attention to detail and strong organizational skills, with the ability to manage multiple projects simultaneously.
- Experience with AMA style or other medical writing styles (e.g., li>
- Experience in regulatory writing, medical journalism, or patient education.
- Background in writing for healthcare marketing or product-related materials (e.g., pharmaceutical marketing, medical device product information).
- Familiarity with digital tools for remote collaboration and project management (e.g., li>
As a medical writer, you will have the flexibility to work remotely and set your own schedule. We offer competitive rates based on your experience level and the scope of each project. If you meet the qualifications and are interested in joining our network of talented medical writers, please submit your resume and a brief writing sample.
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