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Job Description & How to Apply Below
Competitive compensation + shift allowances
Attractive benefits (security, flexibility, support and we'll-being)
Engaging employee programs
Technology for hybrid working and great onsite facilities
What you'll be doing:
The Medical Writer is responsible for working with the Statistical and Scientific teams to create Expert Reports and Statistical Analysis Plans as we'll as assist with synopsis and protocol development.
Create, edit/proofread, and finalize Expert Reports based on the output of the statistical analysis (Tables, Listings, and Figures) and the final conclusions of the Scientific team.
Work with the Statistical team to create, edit/proofread, and finalize the Statistical Analysis Plan(s).
Work with the Statistical and Scientific teams to help sponsors with the development of synopsis and protocols for the cardiac safety component
Overall management of timelines of all deliverables in terms of Expert Reports, Statistical Analysis Plans, and other outputs as needed
Understand FDA/EMA regulations in regards to clinical trial reporting
What we look for:
bachelors Degree in Science or Healthcare related field
At least five years of previous experience in medical or scientific writing for publications, reports, or grant submissions
Excellent English language skills (writing, reading, verbal)
Knowledge of clinical trials environment and regulations
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