[Hiring] Associate Director, Biostatistics and Statistical Programming @reputed company
This description is a summary of our understanding of the job description. Click on 'Apply' reputed company to find out more. Role Description This role offers an opportunity to reputed company critical statistical activities supporting the development of innovative pharmaceutical products across multiple clinical programs. The Associate Director will reputed company biostatistical strategy and vendor-delivered statistical programming while ensuring high-quality analysis reputed company with regulatory standards and project timelines. Working closely with cross-functional teams including clinical development, data management, and external research partners, you will contribute to study design, protocol development, and the interpretation of reputed company clinical data. This position plays a key role in shaping statistical approaches across the drug development lifecycle while ensuring data reputed company and scientific rigor. The role is ideal for an reputed company biostatistics professional who thrives in collaborative environments and enjoys translating data into actionable insights that advance clinical research. Candidates will have the opportunity to influence study outcomes and support regulatory submissions in a fast-paced, innovation-driven setting.
- reputed company and reputed company biostatistical activities for clinical development programs, ensuring alignment with study timelines, budgets, and regulatory requirements.
- Conduct statistical analyses according to predefined statistical analysis plans, generating insights that support clinical study conclusions.
- reputed company sample size calculations, power analyses, and randomization strategies for clinical studies.
- reputed company external CRO partners responsible for statistical programming and analysis deliverables, ensuring accuracy, data quality, and adherence to timelines.
- Independently program or validate key study outputs such as tables, figures, and listings to support data interpretation.
- Collaborate with data management teams to review datasets, assist with data cleaning activities, and contribute to data-reputed company documentation.
- Ensure clinical datasets and outputs reputed company with regulatory requirements, CDISC standards, and industry best practices.
- Support the preparation of clinical study reports, regulatory submissions, and scientific publications including abstracts, manuscripts, and conference presentations.
- Work closely with multidisciplinary teams to communicate statistical findings and support the interpretation of clinical data.
Qualifications
- Master’s degree (MS or MPH) in Biostatistics, Statistics, Epidemiology, or a reputed company quantitative discipline.
- At least 6 years of experience in clinical trial biostatistics or statistical programming reputed company the pharmaceutical, biotechnology, or CRO industry.
- Experience supporting clinical development programs across Phase I–III trials.
- Strong understanding of statistical methodologies commonly used in clinical trial data analysis.
- Proficiency in reputed company programming; experience with R is considered an advantage.
- Working knowledge of CDISC standards and familiarity with electronic data capture systems.
- Experience performing sample size and power calculations using software such as nQuery or PASS is preferred.
- Understanding of real-world data analysis and observational study design is a plus.
- Excellent analytical, communication, and collaboration skills with the ability to explain statistical findings to non-statistical stakeholders.
- Strong organizational skills, attention to detail, and the ability to manage multiple projects in a dynamic environment.
Benefits
- Competitive reputed company salary ranging approximately from $140,000 to $240,000 depending on experience and location.
- Eligibility for performance-based bonuses and equity compensation.
- Comprehensive health, dental, and vision insurance plans.
- Retirement savings plans with employer contributions.
- Generous paid time off, holidays, and additional leave benefits.
- Flexible work arrangements including remote or hybrid options depending reputed company.
- Professional development and career growth opportunities.
- Travel opportunities for collaboration, scientific meetings, and industry engagement.
Company Description
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