Biostatistics Director

Biostatistics Director

ICON

Multiple Locations

What You Will Be Doing:

• Designing and implementing statistical analysis plans for clinical trials, ensuring alignment with study objectives and regulatory guidelines.
• Overseeing the statistical analysis of clinical data, providing insights and interpretations to support decision-making and reporting.
• Collaborating with cross-functional teams, including clinical, regulatory, and data management, to ensure integrated and efficient study execution.
• Mentoring junior statisticians and providing training on statistical methodologies and software applications.
• Contributing to the preparation of regulatory submissions and publications, ensuring statistical rigor and transparency.
• Staying updated on industry trends and advancements in statistical methodologies to drive innovation in study design and analysis.
• Participating in protocol development and providing input on endpoints and statistical considerations for clinical studies.

Your Profile:

• A master’s degree or Ph.D. in Biostatistics, Statistics, or a related field.
• Extensive experience in biostatistics within the pharmaceutical or biotech industry, particularly in clinical trial design and analysis.
• Strong knowledge of statistical software (e.g., SAS, R) and proficiency in programming for data analysis.
• Excellent problem-solving skills, with the ability to interpret complex data and provide actionable insights.
• Demonstrated leadership abilities, with experience in mentoring and guiding teams.
• Strong communication skills, with the ability to present statistical concepts to non-statistical audiences effectively.
• Detail-oriented, with excellent organizational skills to manage multiple projects and meet deadlines in a fast-paced environment.