Immunovant, Inc.
Immunovant, Inc. is a clinical-stage immunology company dedicated to enabling normal lives for people with autoimmune diseases. As trailblazer in anti-FcRn technology, the Company is developing innovative, targeted therapies to meet the complex and variable needs of people with autoimmune diseases.
The Role Reporting to the Executive Director, Biostatistics, this position is responsible for collaborating with both internal and external stakeholders to deliver the execution of our Biostatistics strategy. The individual in this position will have the unique opportunity to participate in the rapid growth of a biotech startup.
Key Responsibilities
Provide statistical inputs into protocol and clinical study report development, statistical analysis plans, interpretation of statistical analysis results, randomization plans.
Provide oversight and review of statistical documents for multiple clinical trials, including TLF shells, eCRFs, specifications of variable derivations, and all deliverables from outside vendors or internal programmers.
Develop effective collaborations with others within clinical teams and partner lines such as Statistical Programming, Data Management, Medical, Clinical Operations, and Regulatory.
Ensure that all study level statistical activities are conducted in compliance with relevant regulatory requirements and Immunovant standards.
Provide planning, delivery and communication of statistical analyses, data presentations, and scientific reports.
Oversight statistics and programming vendors.
Open to opportunities to utilize innovative statistical methodology to streamline the clinical development process and facilitate optimal decision‑making.
Requirements
PhD or MS in Statistic, Biostatistics, Mathematics, or related field.
5+ years (7+ years for MS) of experience in biotechnology, pharmaceutical or health‑related area.
Knowledge of relevant FDA, EU, ICH guidelines and regulations.
Understanding of drug development.
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.
Remote‑based; access to Immunovant’s NYC and North Carolina offices available.
Domestic or international travel may be required ( $190,000 - $210,000 USD.
Compensation is based on a number of factors, including market location, and may vary depending on job‑related knowledge, skills, and experience. Equity and other forms of compensation may be provided as part of a total compensation package, in addition to a full range of medical, dental, vision, 401k, and other benefits, including unlimited paid time off and parental leave.
As set forth in IMVT Corporation’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law.
#J-18808-Ljbffr
The Role Reporting to the Executive Director, Biostatistics, this position is responsible for collaborating with both internal and external stakeholders to deliver the execution of our Biostatistics strategy. The individual in this position will have the unique opportunity to participate in the rapid growth of a biotech startup.
Key Responsibilities
Provide statistical inputs into protocol and clinical study report development, statistical analysis plans, interpretation of statistical analysis results, randomization plans.
Provide oversight and review of statistical documents for multiple clinical trials, including TLF shells, eCRFs, specifications of variable derivations, and all deliverables from outside vendors or internal programmers.
Develop effective collaborations with others within clinical teams and partner lines such as Statistical Programming, Data Management, Medical, Clinical Operations, and Regulatory.
Ensure that all study level statistical activities are conducted in compliance with relevant regulatory requirements and Immunovant standards.
Provide planning, delivery and communication of statistical analyses, data presentations, and scientific reports.
Oversight statistics and programming vendors.
Open to opportunities to utilize innovative statistical methodology to streamline the clinical development process and facilitate optimal decision‑making.
Requirements
PhD or MS in Statistic, Biostatistics, Mathematics, or related field.
5+ years (7+ years for MS) of experience in biotechnology, pharmaceutical or health‑related area.
Knowledge of relevant FDA, EU, ICH guidelines and regulations.
Understanding of drug development.
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.
Remote‑based; access to Immunovant’s NYC and North Carolina offices available.
Domestic or international travel may be required ( $190,000 - $210,000 USD.
Compensation is based on a number of factors, including market location, and may vary depending on job‑related knowledge, skills, and experience. Equity and other forms of compensation may be provided as part of a total compensation package, in addition to a full range of medical, dental, vision, 401k, and other benefits, including unlimited paid time off and parental leave.
As set forth in IMVT Corporation’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law.
#J-18808-Ljbffr