Description
As a Senior Principal Biostatistician at ICON, you will lead statistical methodologies and contribute to designing and analysing clinical studies to ensure high data integrity and regulatory compliance.
Key Responsibilities:
- Design and implement statistical analysis plans for clinical trials aligned with study objectives and regulatory guidelines.
- Oversee statistical analysis of clinical data, providing insights to support decision-making and reporting.
- Collaborate with cross-functional teams to ensure integrated study execution.
- Mentor junior statisticians and provide training on statistical methodologies and software applications.
- Contribute to regulatory submissions and publications, ensuring statistical rigor and transparency.
- Stay updated on industry trends and advancements in statistical methodologies.
- Participate in protocol development and provide input on endpoints and statistical considerations.
Requirements:
- Master's degree or Ph.D. in Biostatistics, Statistics, or a related field.
- Extensive experience in biostatistics within the pharmaceutical or biotech industry.
- Strong knowledge of statistical software (e.g., SAS, R) and programming skills.
- Excellent problem-solving skills and ability to interpret complex data.
- Demonstrated leadership abilities and experience in mentoring teams.
- Strong communication skills, with the ability to present statistical concepts effectively.
- Detail-oriented with excellent organisational skills.
Rewards & Benefits:
- Competitive base salary and performance-related incentives.
- Health and wellbeing programmes, including medical, dental, and vision coverage.
- Retirement and pension plans.
- Life assurance and disability coverage.
- Employee assistance programmes and wellbeing resources.
- Learning and development opportunities.