We have a current opportunity for an Associate Director, Biostatistics!
The AD, Biostatistics will be a core member of the cross-function team, contributing to and supporting the activities/projects within clinical study design and analysis, protocol development, analysis planning, etc.
Responsibilities:
- Contribute to all aspects of development strategy
- Develop collaborative relationships and works effectively with biostatistics lead and other cross-functional team members
- Oversees all biostatistics activities for one (or more) clinical programs to ensure timely and accurate delivery of statistical designs, analyses, and regulatory submissions
- Provides statistical input to drug development, including development plans, complex study designs, statistical methodology, etc.
Qualifications:
- PhD or Masters in Biostatistics, Mathematics, Applied Statistics, or related field
- At least 5 to 7 years of relevant experience, relative to degree
- Broad knowledge and understanding of advanced statistical concepts and techniques
- Familiarity and experience with regulatory guidelines for drug development, submissions, and statistical practices
- Understanding of the drug submission and approval process regionally and globally
- Excellent interpersonal, communication, writing and organizational skills
Reach out to learn more!