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Medical Writer II
| Company | Icon |
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| Location | Plainview, NY, USA |
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| Salary | $83032 – $103790 |
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| Type | Full-Time |
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| Degrees | Bachelor’s |
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| Experience Level | Mid Level |
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Requirements
- Bachelor’s degree in Life Sciences, Pharmacy, Medicine, or related field
- Minimum of 3 years of experience in medical writing within the pharmaceutical, biotechnology, or contract research organization (CRO) industry
- Proficiency in scientific and medical terminology
- Excellent written and verbal communication skills
- Attention to detail
- Strong analytical and critical thinking skills
- Familiarity with regulatory requirements, industry guidelines, and publication standards governing the preparation and submission of clinical trial documents and scientific manuscripts
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
Responsibilities
- Collaborating with cross-functional teams to prepare, write, and edit clinical study reports (CSRs), clinical protocols, investigator brochures (IBs), patient narratives, and other regulatory documents in compliance with internal standards and regulatory guidelines
- Conducting literature reviews, data analysis, and interpretation of clinical trial results to support the development of scientific manuscripts, abstracts, posters, and presentations for publication in peer-reviewed journals and scientific conferences
- Assisting in the review and validation of clinical data, ensuring accuracy, completeness, and consistency with study protocols, standard operating procedures (SOPs), and regulatory requirements
- Participating in project meetings, teleconferences, and client interactions to discuss project objectives, timelines, and deliverables, while providing input and feedback on document content, format, and presentation
- Keeping abreast of emerging trends, scientific developments, and regulatory updates in relevant therapeutic areas, and applying knowledge of medical writing principles and best practices to support the successful execution of clinical research projects.
Preferred Qualifications
- Familiarity with document management systems, reference management software, and statistical analysis tools preferred.
