Senior Statistical Advisor-Canada

The Senior Statistical Advisor will provide strategic statistical guidance and scientific leadership across clinical development programs, supporting rigorous trial design, analysis, and interpretation to inform decision-making. The role will serve as a senior scientific resource for sponsors and internal teams, address complex methodological challenges, provide scientific mentoring, and contribute statistical expertise to regulatory submissions and agency interactions.

Brand name:
Indero

Our company:

The work environment

At Indero, you will work with brilliant and driven colleagues. Our values are integrity, commitment and teamwork. We offer a stimulating work environment and attractive advancement opportunities.

As a Senior Statistical Advisor, you will be eligible for the following perks:

• Flexible work schedule
• Permanent full-time position
• Complete benefits (medical, dental, vision, RRSP, vacation, personal days, virtual medical clinic, public transportation rebates, social activities)
• Ongoing learning and development

About Indero

Indero is a contract research organization (CRO) specialized in dermatology with a team of over 350 employees. Since its beginnings in 2000, our organization has benefited from a solid reputation for the quality of its research and services exceeding the expectations of its clients. Based in Montreal, Indero continues to grow and expand in North America.

Indero is committed to providing equitable treatment and equal opportunity to all individuals. As such, Indero will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.

We thank you for your application and please note that only those selected for an interview will be contacted.

Indero only accepts applicants with a work permit for Canada.

More specifically, the Senior Statistical Advisor must:

• Provide strategic statistical input into clinical development plans, trial protocols, and other research projects, recommending scientifically rigorous, efficient, and cost-effective designs and appropriate statistical methods.
• Develop SAPs for complex studies and provide peer review for SAPs and TLF Shells for clinical trials.
• Resolve complex statistical issues and provide scientifically sound, practical recommendations.
• Interpret clinical trial results and communicate statistical concepts, findings, and their implications clearly to technical and non-technical audiences to inform decision-making.
• Provide statistical expertise for regulatory submissions, agency interactions, and responses to regulatory queries, in collaboration with sponsors and cross-functional teams.
• Contribute to the development of abstracts, manuscripts for peer-reviewed publication, posters, and scientific presentations.
• Provide scientific mentoring and training to biostatisticians and statistical programmers to strengthen methodological expertise and statistical judgment and ensure alignment with applicable ICH guidelines, regulatory requirements, and company standards.
• Serve as an independent unblinded biostatistician supporting IDMC reviews and/or interim analyses, as appropriate, in accordance with applicable charters, analysis plans, and blinding procedures.
• Maintain current knowledge of statistical methodologies, industry standards, and regulatory guidance, and assess their implications for statistical practice.

Employee may be assigned to other responsibilities that do not pertain to their former description, if they havE the required experience, are qualified and/or have received adequate training.