Senior Director, Biostatistics

🔥 4 hours ago

Apply Now

Find Similar Remote Jobs

Receive Emails For Remote Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Immunovant

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2018

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

Immunovant is a company focused on advancing treatments for autoimmune diseases through a patient-focused approach. With a vision of enabling normal lives for people with autoimmune diseases, Immunovant applies its expertise in science to develop and test new therapies. The company emphasizes complex and variable needs across different stages and severities of diseases. Immunovant is committed to pushing forward its therapeutic areas and clinical trials, while also engaging with patients, caregivers, and investors about their ongoing studies and corporate initiatives.

📋 Description

• Provide oversight and contributions to statistics strategy, planning, execution, and communication for programs as assigned. • Provide scientifically rigorous statistical input into clinical development plans, protocol development, statistical analysis plans, regulatory submissions and questions, interpretation of statistical analysis results, and other product support initiatives. • Develop effective collaborations with others within clinical teams and partner lines (such as Medical Directors and Regulatory). • Ensure that all study and project level statistical activities are conducted in compliance with relevant regulatory requirements and Immunovant standards. • Identify opportunities to utilize innovative statistical methodology to streamline the clinical development process and facilitate optimal decision-making. • Manage indication/study biostatisticians.

🎯 Requirements

• PhD. in Statistic, Biostatistics, Mathematics or related field • 12+ years of experience in biotechnology, pharmaceutical or health related area • Knowledge of relevant Health Authority and ICH guidelines, as well as regulations • Demonstrated experience in engaging with Health Authorities • Comprehensive understanding of drug development from Phase 2 to launch • Demonstrated ability to collaborate with diverse sets of stakeholders • Strong written and oral communication skills with attention to detail • Desire to work in a fast-paced, innovative environment • Natural collaborator who enjoys working on a cross-functional team

🏖️ Benefits

• full range of medical, dental, vision • 401k • unlimited paid time off • parental leave