Senior Medical Writer – Sr. Manager / Associate Director
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Job Description
Senior Medical Writer developing clinical documentation and leading projects at Pfizer. Collaborating with cross-functional teams and ensuring compliance in drug development processes.
Responsibilities:
- Develop and lead complex projects, creating comprehensive plans to meet objectives.
- Collaborate with clinicians, statisticians, and clinical scientists to author protocols and drive document strategies.
- Independently organize, analyze, and interpret scientific, clinical, and statistical data to prepare key clinical documents.
- Suggest improvements to document processes or templates to enhance quality and efficiency.
- Review the work of others in Sub Business Unit/Sub Operating Unit.
Requirements:
- BA/BS with strong experience or MBA/MS with 5+ years of experience or PhD/JD with some experience or MD/DVM with any years of relevant experience
- Demonstrated ability to interpret and apply guidelines to document writing, with a comprehensive understanding of the drug development process and regulatory knowledge
- Excellent project management skills to organize work and handle multiple projects simultaneously
- Experience with software commonly used to present and analyze data, such as Word, PowerPoint, and Excel
- Strong analytical and problem-solving skills
- Exceptional written and verbal communication skills
Benefits:
- Health insurance
- Professional development opportunities
- Flexible working hours
- Remote work options
- Paid time off
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