Skills

Communication Teamwork Training Programming Process Improvement Mathematics

Job Specifications

Key Responsibilities

Develop and maintain SAS programs for generating ADaM datasets and TFLs.
Perform quality control and validation on programs developed by others.
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.

Qualifications

Bachelor’s or above in Statistics, Biostatistics, Mathematics, Computer Science, or related field.
1–2 years of SAS programming experience in clinical trials (pharma or CRO preferred).
Strong understanding of clinical trial statistics and regulatory guidelines.
Ability to work independently on assigned projects.
Proficiency in Microsoft Office and statistical software.
Good communication skills in English (written and spoken).
Strong teamwork and documentation skills.

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, w... Know more