Medical Writer
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Job Location:
Beachwood, OH - USA
Monthly Salary:
Not Disclosed
Posted on:
5 hours ago
Vacancies:
1 Vacancy
Job Summary
We are seeking a detail-oriented and scientifically savvy Remote Medical Writer to join our this role you will be responsible for creating clear accurate and engaging medical and scientific content tailored to healthcare professionals patients regulatory bodies and internal stakeholders. This position is ideal for someone who can translate complex clinical information into accessible high-quality written materials.
Key Responsibilities
- Develop write and edit medical and scientific documents including:
- Clinical study reports (CSRs) protocols investigator brochures
- Manuscripts abstracts and conference posters
- Continuing medical education (CME) materials
- Medical marketing content (brochures white papers slide decks)
- Patient education materials
- Ensure all content is accurate evidence-based and aligned with industry regulatory and company standards.
- Interpret and synthesize clinical data from research studies scientific literature and internal sources.
- Collaborate with cross-functional teams including medical affairs regulatory clinical operations marketing and subject-matter experts.
- Maintain awareness of relevant therapeutic areas clinical guidelines and regulatory requirements.
- Apply consistent editorial style and formatting across documents.
- Manage multiple projects and meet deadlines in a remote self-directed environment.
Qualifications
- Bachelors Masters or PhD in Life Sciences Medicine Pharmacy Nursing Public Health or related field.
- Proven experience as a medical writer (agency clinical research pharmaceutical or academic setting preferred).
- Strong understanding of clinical research principles medical terminology and scientific methodology.
- Excellent written communication editing and data interpretation skills.
- Ability to explain complex medical information clearly to diverse audiences.
- Familiarity with AMA style and similar editorial guidelines (e.g. ICH GPP).
- Proficiency with common writing and data tools (Microsoft Office reference managers etc.).
- Ability to work independently manage time effectively and collaborate virtually.
Preferred Skills
- Experience with regulatory writing (FDA/EMA submissions).
- Knowledge of specific therapeutic areas (e.g. oncology cardiology neurology).
- Understanding of publication planning and medical communications processes.
- Ability to create visually engaging scientific presentations.
- Experience working in an agency or fast-paced project environment.
What We Offer
- Fully remote flexible work environment.
- Competitive compensation and benefits.
- Opportunities for professional development and advancement.
- Collaborative and supportive team culture.
Company Industry
IT Services and IT Consulting
Key Skills
- Clinical Research
- Adobe Acrobat
- FDA Regulations
- Technical Writing
- Biotechnology
- Clinical Development
- Clinical Trials
- Microsoft Powerpoint
- Research Experience
- Document Management Systems
- Word Processing
- Writing Skills
