Senior Manager, Statistics / Senior Clinical Statistician

TL;DR

Senior Manager, Statistics / Senior Clinical Statistician (Clinical Biostatistics): Providing statistical expertise for clinical trial design, analysis, reporting, and regulatory submissions with an accent on experimental design, statistical methodology, and scientifically robust evidence. Focus on designing analysis strategies, interpreting complex clinical data, supporting health authority interactions, and delivering compliant statistical outputs for assigned studies and projects.

Location: Onsite in Shanghai, China

Company

hirify.global is a pharmaceutical company focused on developing medicines and generating evidence to support safe and appropriate patient care.

What you will do

• Provide statistical input into study designs, statistical analysis plans, project development plans, and regulatory submission strategies.
• Plan, deliver, and communicate statistical analyses, clinical trial results, topline results, exploratory analyses, and meta-analyses.
• Prepare scientific reports, publications, presentations, and responses to regulatory queries.
• Own study-level and submission-level statistical deliverables for assigned projects.
• Collaborate with clinical research functions, project statisticians, statistical leaders, and external regulatory, academic, and industry organizations.
• Research statistical methodologies, resolve moderately complex problems, and lead innovative projects across business units.

Requirements

• PhD with at least one year of statistical consultation experience.
• Demonstrated experience delivering high-quality statistical contributions and scientific reports for clinical trials supporting regulatory submissions.
• Deep knowledge of experimental design and the ability to apply relevant scientific literature.
• Strong written and verbal communication skills.
• Experience developing and managing plans to achieve objectives.
• Ability to work independently in ambiguous situations and make decisions on moderately complex problems.

Nice to have

• Pharmaceutical industry experience and expertise in biostatistical methodologies for clinical trials.
• Experience with regulatory submissions and health authority interactions.
• Strong project management, collaboration, teamwork, and problem-solving skills.
• Experience using generative AI tools such as ChatGPT or Microsoft Copilot, with awareness of responsible AI practices.

Culture & Benefits

• On-premise work arrangement in Shanghai.
• Opportunities to contribute to global healthcare outcomes through scientifically robust evidence.
• Professional development opportunities within and outside the organization.
• Work across clinical research, regulatory, academic, and industry collaborations.