Job Description
- Job Description:
- Serve as primary author who writes and provides input on routine documents such as clinical study reports and study protocols, and summarizes data from clinical studies
- May assist with more complex clinical and scientific and program level documents, including IBs, INDs, and MAAs
- Ensure compliance with quality processes and requirements for assigned documents
- May assist in determining best practices, methods and techniques for achieving optimal results
- May assist in program management activities
- Requirements:
- Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years)
- Experience in neurology preferred
- Experience working in the pharmaceutical/CRO industry preferred
- Experience in scientific writing advantageous
- Benefits:
- Health insurance
- Paid time off
- Flexible work arrangements
- Professional development opportunities
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