Job Purpose:

SAS Programming Team in the department of Statistics of Hengrui R&D Center provides clinical programming support for various clinical studies and contributes to the development of departmental standards. Senior Manager of SAS Programming is accountable for programming team deliverables for the assigned clinical projects. This role is that of a programming lead who plans and provides oversight of SAS programming activities (e.g., development, verification and documentation) in support of clinical trial reporting and submissions.

Duties& Responsibilities

1. Participates in review of protocol, statistical analysis plan (SAP), data integrity plan (DIP), data management plan (DMP) and case report form (CRF).

2. Participates in creation of programming documents including list of tables, mock tables, analysis specifications, dataset specifications and other related documents, and ensures all programming-related files are in the appropriate location on the company server.

3. Is accountable for the production of high-quality, on-time statistical programming deliverables (such as datasets and tables/listings/figures (TLFs)) for either outsourced or insourced clinical studies and development programs.

4. Works with data management to perform data quality checks.

5. Ensures clear and timely communications with study team members.

6. Ensures all programming activities following regulatory requirements and company SOPs.

7. Mentors new hires or provide training to SAS programmers.

8. Participates in the development and implementation of programming tools for data analysis and reporting.

9. Contributes to development of programming related SOPs.

10. Provides regular oversight of statistical programming work outsourced to programming vendors/CROs and acts as a liaison between the vendor/CRO and the Hengrui Biostatistics and Programming function.

Job Requirements

1. Minimum of a Bachelor’s degree in Statistics, Mathematics, Computer Science, Pharmaceuticals Sciences, Life Sciences, Public Health or other related areas. Master's Degree is preferred.

2. In-depth knowledge of SAS programming, statistics, clinical drug development process and regulatory requirements related to the role;

3. In-depth knowledge of Base SAS, SAS/STAT, SAS Graph, SAS SQL and SAS Macro Language. SAS Certification is preferred, not required.

4. Effective communication skills and ability to establish and maintain effective working relationships with study team members. Being fluent in spoken and written English.

5. Must be a motivated, self-directed learner with a passion and drive for technology.

6. Ability to work under pressure and manage multiple projects simultaneously.

上班地址：海科路1288号