Tigermed

About the Company

Tigermed (Stock code: 300347.SZ/3347.HK) is a leading provider of innovative clinical research solutions across the full life cycle of biopharmaceutical and medical device products globally. With a broad portfolio of services and a promise of quality, from clinical development to commercialization, we are committed to moving our customers and patients through their development journey efficiently and cost-effectively. Tigermed currently represents a worldwide network of more than 100 subsidiaries and 180 service locations, with over 10,000 employees across 50 countries in Asia Pacific, Europe, North & South America and Africa. We are devoted to building an integrated platform that enables boundless possibilities for healthcare industry, embracing challenges to fulfill our commitment to serve unmet patients’ needs, and eventually saving lives.

Listed Jobs

Company Name

Tigermed

Job Title

Senior Statistical Analyst I

Job Description

Job title: Senior Statistical Analyst I Role Summary: Leads and develops ADaM datasets and TFLs in SAS, overseeing programming projects, ensuring compliance with CDISC/IAT-GCP, and providing technical guidance to junior analysts. Expactations: Deliver accurate, compliant outputs; manage programming deliverables, mentor team members, and serve as primary programming liaison with clients. Key Responsibilities: - Design and validate ADaM datasets and TFLs using SAS. - Draft, review, and maintain programming specifications and documentation. - Develop reusable macros and tools for workflow efficiency. - Lead programming teams: assign tasks, track timelines, and provide mentorship. - Act as the principal programming contact with clients; deliver outputs and incorporate feedback. - Conduct SAS code reviews, document issues, and enforce quality standards. - Archive all deliverables and documentation following SOPs. - Support professional development of team members. Required Skills: - Proficient in SAS programming and macro development. - Solid understanding of clinical trials, statistical methods, and regulatory requirements. - Experience leading programming projects and mentoring staff. - Strong communication skills for global client and team interactions. - Competence in Microsoft Office suite. Required Education & Certifications: - Bachelor’s degree (or higher) in Statistics, Mathematics, Computer Science, or related discipline. - Minimum 3 years of SAS programming experience in pharmaceutical or CRO settings.

Canada

Remote

Senior

09-03-2026

Company Name

Tigermed

Job Title

Statistical Analyst

Job Description

**Job title** Statistical Analyst **Role Summary** Design, develop, and validate ADaM datasets and treatment‐full line (TFL) files using SAS, ensuring compliance with regulatory standards and internal SOPs. Provide robust support for clinical trial data management, collaborate cross‑functionally, and foster continuous process improvement. **Expectations** - Deliver accurate SAS programs and data sets within project timelines. - Maintain high quality control standards and adhere to SOP/WPD compliance. - Lead documentation and specification creation for programming deliverables. - Participate in ad‑hoc data requests, clinical data reviews, and validation activities. **Key Responsibilities** - Develop and maintain SAS programs for ADaM datasets and TFLs. - Perform quality control and validation on colleagues’ programs. - Collaborate with statisticians and data managers to ensure data accuracy and consistency. - Create and maintain programming specifications and supporting documents. - Participate in SOP/WPD compliance and continuous process improvement initiatives. - Support ad‑hoc data requests, clinical data reviews, and data validation activities. - Continuously improve programming and clinical trial knowledge through training and mentoring. **Required Skills** - Proficient SAS programming (including macro usage). - Strong understanding of ADaM, SDTM, and clinical trial regulatory guidelines. - Ability to perform program validation and quality control. - Excellent documentation and specification writing skills. - Independent work capability and strong time‑management. - Proficiency with Microsoft Office (Word, Excel, PowerPoint). - Effective verbal and written communication in English. - Team‑orientated, collaborative mindset. **Required Education & Certifications** - Bachelor’s degree (or higher) in Statistics, Biostatistics, Mathematics, Computer Science, or a related field. - 1–2 years of SAS programming experience in clinical trials (pharma or CRO preferred). - No specific certifications required, but familiarity with industry regulatory standards is preferred.

Canada

Remote

09-03-2026