![Building A Digital PR Strategy: 10 Essential Steps for Beginners [With Examples]](https://buzzsumo.com/wp-content/uploads/2023/09/Building-A-Digital-PR-Strategy-10-Essential-Steps-for-Beginners-With-Examples-bblog-masthead.jpg)
![How One Brand Solved the Marketing Attribution Puzzle [Video]](https://contentmarketinginstitute.com/wp-content/uploads/2025/03/marketing-attribution-model-600x338.png?#)
![How to Use GA4 to Track Social Media Traffic: 6 Questions, Answers and Insights [VIDEO]](https://www.orbitmedia.com/wp-content/uploads/2023/06/ab-testing.png)
![[Hybrid] Graphic Designer in Malaysia](https://a5.behance.net/920d3ca46151f30e69b60159b53d15e34fb20338/img/site/generic-share.png)
Virology Biostatistics Director
A company is looking for a Director of Biostatistics - Virology. Key Responsibilities: Provide statistical leadership for Virology clinical trials, including trial design and decision support Act as the statistical lead for specific Virology molecules during Health Authority interactions Collaborate with cross-functional teams to ensure timely statistical data analysis and reporting for clinical trials Required Qualifications: PhD with 8+ years, Master's Degree with 10+ years, or Bachelor's Degree with 12+ years of statistical analysis experience in the pharmaceutical or biotechnology industry (or at a CRO) Industry experience in statistical analysis of biomedical data using statistical software (SAS and R preferred) Extensive experience in drug development, including design and analysis of phase 1-3 trials and participation in NDA/BLA filing Demonstrated ability to lead high-performing teams and manage internal and external resources effectively Experience in overseeing technical and operational statistical activities for clinical trials
A company is looking for a Director of Biostatistics - Virology.
Key Responsibilities:
Provide statistical leadership for Virology clinical trials, including trial design and decision support
Act as the statistical lead for specific Virology molecules during Health Authority interactions
Collaborate with cross-functional teams to ensure timely statistical data analysis and reporting for clinical trials
Required Qualifications:
PhD with 8+ years, Master's Degree with 10+ years, or Bachelor's Degree with 12+ years of statistical analysis experience in the pharmaceutical or biotechnology industry (or at a CRO)
Industry experience in statistical analysis of biomedical data using statistical software (SAS and R preferred)
Extensive experience in drug development, including design and analysis of phase 1-3 trials and participation in NDA/BLA filing
Demonstrated ability to lead high-performing teams and manage internal and external resources effectively
Experience in overseeing technical and operational statistical activities for clinical trials