Medical Writer II
ICON plc
full-time
Posted on:
Location Type: Hybrid
Location: Shanghai • China
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About the role
- 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
- Conducting literature reviews, data analysis, and interpretation of clinical trial results
- Assisting in the review and validation of clinical data
- Participating in project meetings, teleconferences, and client interactions
- Keeping abreast of emerging trends, scientific developments, and regulatory updates in relevant therapeutic areas.
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 and ability to convey complex information clearly
- Strong analytical and critical thinking skills
- Familiarity with regulatory requirements, industry guidelines, and publication standards
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and familiarity with document management systems, reference management software, and statistical analysis tools preferred.
Benefits
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Applicant Tracking System Keywords
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Hard Skills & Tools
medical writingdata analysisclinical study reportsclinical protocolsinvestigator brochurespatient narrativesscientific terminologyregulatory documentsanalytical skillscritical thinking
Soft Skills
written communicationverbal communicationattention to detailability to convey complex informationcollaborationclient interaction