
Senior Clinical Trials Medical Writer
15 hours ago
Medical Writer (Clinical Trials)
About the RoleThe Medical Writer is responsible for working with cross-functional teams to develop high-quality reports and analysis plans. This includes creating, editing, and finalizing Expert Reports based on statistical analysis and scientific conclusions.
Main Responsibilities:- Collaborate with Statistical and Scientific teams to create Expert Reports and Statistical Analysis Plans.
- Develop synopsis and protocols for cardiac safety components.
- Manage timelines and deliverables for Expert Reports, Statistical Analysis Plans, and other outputs.
This role requires a strong understanding of FDA/EMA regulations and clinical trials environment.
Requirements- Bachelor's Degree in Science or Healthcare-related field.
- At least 5 years of experience in medical or scientific writing.
- Excellent English language skills (writing, reading, verbal).
- Knowledge of clinical trials environment and regulations.
- Competitive compensation package.
- Attractive benefits including security, flexibility, support, and well-being.
- Engaging employee programs.
- Technology for hybrid working and great onsite facilities.
We are a team of professionals dedicated to delivering high-quality services in the clinical trials industry.
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