
Senior Biostatistician
2 days ago
Responsibilities
- May supervise Biostatisticians, Associate Biostatisticians and SAS programmers (all levels) and direct their work on clinical research studies.
- Provides expert consultation to projects across the company on statistical methodology.
- Solves problems of complex statistical scope.
- Provides technical review of proposed statistical design for research studies across company.
- Serves as the lead Biostatistician on one or more study projects.
- Participates in statistical process development and improvement across company.
- May present at statistical conferences.
- Provides sound strategic, scientific and statistical input to support client’s research projects.
- Leads the project team’s development of study analysis plans and statistical programs to perform analyses and display study data.
- Keeps abreast with current statistical and medical literature to ensure that sound methodologies are adopted.
- Fosters innovation in Biostatistics that will continuously enhance current statistical knowledge and practices.
- Ensures the scientific integrity of the research project and the accuracy of the reported results.
- Performs sample size calculation and provides leadership in the statistical design of research projects.
- Reviews protocols and case report forms to ensure that protocol objectives are met, and standards are maintained.
- Develops study assignment allocation schemas along with appropriate documentation.
- Leads the development of the methods and results sections of clinical study reports and scientific publications.
- Represents Client on behalf of clients at regulatory meetings.
- Provides expertise in methodological advances both internally and externally to improve statistical methodologies.
- Participate in the development and updating of Standard Operating Procedures.
- Other duties as assigned
Qualifications
- MS in biostatistics, statistics, or PhD in biostatistics, statistics, epidemiology or related field
- At least 4 years of related experience with MS or 1 year of related experience with PhD is expected but not required.
- Experience with methodological statistical research, including publication and/or presentation of work in statistical methods development.
- Demonstrated proficiency with statistical methods and applications in clinical research.
- Strong programming skills in SAS and/or R.
- Expertise in state-of-the-art data manipulation and statistical methodology.
- Excellent communication, interpersonal and organization skills.
- Ability to manage multiple tasks.
- Ability to work independently, as well as in a team environment.
- Ability to effectively communicate complex statistical concepts, both written and oral.
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