Job Summary
A company is looking for a Medical Writer Consultant for a 12-month contract with the possibility of extension.
Key Responsibilities:
- Support preparation of regulatory submissions with a focus on oncology trials
- Develop, write, and edit various clinical documents, including protocols and reports
- Collaborate with clients and internal teams to ensure accuracy of content and compliance with standards
Required Qualifications:
- Advanced degree in medical science or life sciences
- 5 to 8 years of relevant experience in oncology clinical research
- Strong understanding of regulatory requirements and oncology therapeutic area
- Knowledge of statistical analysis and presentation of clinical data
- Proficiency in Microsoft Office Suite and familiarity with medical writing software
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