Position: TEMP Medical Writer II Location: Aliso Viejo, CA (Onsite) Employment Type: Contract (W2) Pay Rate: $40/hr - $44/hr on W2 Duration: 6 Months
About the Role
We are seeking a Medical Writer II to support clinical and regulatory documentation activities for current and pipeline medical device products. This role will collaborate with Clinical, Regulatory, and R&D teams to develop high-quality scientific documents while ensuring compliance with regulatory standards.
Key Responsibilities
Prepare and support Clinical Study Reports (CSRs), study protocols, abstracts, posters, and scientific presentations
Translate clinical data into clear, accurate, and regulatory-compliant documents
Review and edit clinical and scientific documents for consistency, quality, and accuracy
Conduct literature searches to support clinical and regulatory submissions
Coordinate conference abstracts, publication timelines, and scientific communications
Develop figures, tables, and presentation materials
Partner with cross-functional teams to manage multiple projects and meet timelines
Qualifications
2–5 years of experience in Medical Writing, Clinical Research, Life Sciences, Medical Devices, Biotechnology, or Pharmaceuticals
Strong understanding of clinical research, medical terminology, and regulatory documentation
Experience with CSRs, protocols, publications, abstracts, or scientific communications
Proficiency in Microsoft Office, Adobe Acrobat, and document management systems
Excellent writing, editing, and organizational skills
Ophthalmology experience is a plus
Education
Bachelor's degree in Life Sciences, Biology, Chemistry, Biomedical Engineering, Pharmacy, Public Health, or related field