A multinational research and development driven pharmaceutical company looking to expand their oncology team. Seeking a senior manager of biostatistics with advanced knowledge of phases I-IV of clinical drug development. Strong candidates would also possess experience in statistical programming language (SAS) as well as exposure to Food and Drug Administration (FDA) submissions.
The Senior Manager of Biostatistics will be responsible for
- Analyzing data across multiple stages of the drug development processes including feasibility assessments, development plans and regulatory submissions
- Creating efficient and effective studies that result in statistically relevant results
- Work independently with regulatory authorities to depict statistical functions
- Play a leadership role throughout the entire clinical drug development process
The Senior Manager of Biostatics will have the following qualifications
- PhD in statistics or biostatistics with at least 3 years of relevant experience or a MS in statistics or biostatics with at least 6 years of relevant experience
- Extensive knowledge of clinical or observational study designs
- Exposure to the pharmaceutical industry
- Experience with FDA regulatory submissions
Benefits
- Remote opportunity, no relocation required
