Remote opportunity at
ImmunovantSenior Manager, Statistical Programming
Immunovant is a clinical-stage biopharmaceutical company focused on developing therapies for individuals with autoimmune diseases using FcRn inhibitor technology. The organization is currently seeking a remote…
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About This Role
Immunovant is a clinical-stage biopharmaceutical company focused on developing therapies for individuals with autoimmune diseases using FcRn inhibitor technology. The organization is currently seeking a remote Senior Manager, Statistical Programming to handle programming and statistical analysis tasks for clinical trials and related research projects. This position involves interpreting trial outcomes, contributing statistical input for results reporting, and overseeing the accuracy of tables, listings, and graphs provided by external contractors. The…
Job Description
Immunovant is a clinical-stage biopharmaceutical company focused on developing therapies for individuals with autoimmune diseases using FcRn inhibitor technology. The organization is currently seeking a remote Senior Manager, Statistical Programming to handle programming and statistical analysis tasks for clinical trials and related research projects.
This position involves interpreting trial outcomes, contributing statistical input for results reporting, and overseeing the accuracy of tables, listings, and graphs provided by external contractors. The professional in this role will collaborate with study teams, participate in vendor evaluations, create derived dataset specifications, and maintain the internal safety database and SAS macro library.
The role operates in a dynamic, fast-paced setting located remotely with headquarters in Durham, NC, and may require domestic or international travel of approximately 10 percent. The compensation range for this full-time opportunity is $175,000 to $195,000 per year, accompanied by a comprehensive benefits package including equity, medical, dental, vision, 401(k), parental leave, and unlimited paid time off.
Responsibilities
- Manage contract research organizations to guarantee analysis deliverables match contractual agreements and resolve data analysis issues with vendor personnel
- Generate timely statistical analyses, programmed outputs, and derived dataset specifications aligned with protocols and statistical analysis plans
- Provide statistical input for scientific publications, presentations, promotional items, statistical analysis plans, and case report forms
- Represent the statistical programming team during study meetings and offer guidance to development teams
- Contribute to the evaluation and selection of external vendors
- Review case report form annotations, analysis plans, and programmed output shells
- Participate in maintaining and developing the internal safety database and SAS macro library
Requirements
- Master's degree with at least 7 years of statistical programming experience in a pharmaceutical, biotechnology, or contract research organization environment, or a Bachelor's degree with a minimum of 10 years of relevant experience
- Proficiency in SAS programming tools including Base SAS, SAS/Stat, SAS/Graph, ODS, and macros, alongside a strong grasp of database systems
- Demonstrated leadership experience with CDISC ADaM, SDTM, and electronic submissions such as define.xml and ADRG/SDRG
- Practical background in clinical trial reporting and data analysis workflows for drug development
- Prior involvement with new drug application or marketing authorization application submissions
- Past experience collaborating with contract research organizations
Qualifications
- Degree in a quantitative science discipline such as Statistics, Mathematics, or Computer Science
- Strong organizational skills with adaptability to shifting priorities
- Excellent interpersonal and communication abilities
Core Skills
Benefits
- Annual salary between $175,000 and $195,000
- Equity and other compensation forms included in the total package
- Comprehensive medical, dental, and vision coverage
- 401(k) plan
- Unlimited paid time off
- Parental leave
Frequently Asked Questions
Answers are based only on the employer’s listing; where it doesn’t say, neither do we.
Is this position remote?
Yes, the posting specifies that the role is remote with headquarters in Durham, NC.
What is the salary range for this job?
The salary range is USD 175,000 to 195,000 per year, with total compensation potentially including equity and other forms of pay.
What education and experience are required?
Candidates must hold either a Master's degree in a quantitative science discipline with at least 7 years of relevant experience, or a Bachelor's degree in a quantitative science discipline with a minimum of 10 years of relevant experience in a biotech, pharmaceutical, or contract research organization environment.
Does the role require any travel?
Yes, domestic or international travel may be required at approximately 10 percent.
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