Job Summary
A company is looking for a Medical Writing Scientist.
Key Responsibilities
- Prepare regulatory documents for novel pharmaceutical products in oncology
- Author and coordinate clinical documents in alignment with internal standards and regulatory requirements
- Participate in cross-functional document planning and review meetings to ensure timely completion of tasks
Required Qualifications
- Master's degree in Biology (Molecular/Cell), Biochemistry, Pharmacy, or related field
- 2 years of experience in the job offered or a related occupation
- Experience in medical writing or regulatory document preparation
- Knowledge of clinical protocols and study reports
- Familiarity with Medical Writing Style Guide and publishing guidelines
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