Statistical Programmer

Saama Technologies; Coimbatore District; On-site; INR 600,000 - 900,000; Full time

Job summary

Saama Technologies in Coimbatore, India is seeking a Statistical Programmer to work independently on SDTM mappings and client-specific mappings. The role involves understanding clinical domain nuances, mapping logic, and data issues, while learning the product and mechanism used for SDTM mapping.

Responsibilities include contributing to mapping specifications, using SAS/R/Python, and ensuring CDISC/regulatory compliant datasets in collaboration with Biostatistics and Data Management teams.

Qualifications

• Clinical domain knowledge and mapping understanding are required.
• CDISC SDTM/ADaM knowledge is expected.

Responsibilities

• Pick up multiple tools/technologies on the job.

Skills

Clinical domain knowledge

CDISC standards familiarity

SAS programming

Python programming

R programming

Communication skills

Team player

Education

Graduation in Pharmacy/Computer Science

Tools

SAS

Python

R

Job description

Statistical Programmer reports to Principal Statistical programmer 3/ Lead, Statistical Programming (L4 (3) or M1) , is responsible to work independently on the most of the Mapping activities (SDTM/Client specific mappings) which are simple and medium complex for assigned client in the given environment for the standard domains. Understanding clinical domain, mapping logic, data issues is a part of this role. Learning the product/system/mechanism to be used for SDTM mapping is a part of this role.

Knowledge, Skills Abilities:

• Clinical Domain knowledge
• Familiarity with CDISC Standards (SDTM Knowledge, ADaM , Submission package)
• SAS Programming (Experience up to 2 years)
• Python Programming will be an added advantage
• R Programming will be an added advantage
• Good Communication skills, learning attitude and good team player

Education and Work Experience:

• Graduation in Pharmacy/Computer Science, or any such equivalent graduation from a reputed institute.

Responsibilities:

• Ability to pick up multiple tools/technologies on the job.
• Import and Export raw data
• Contribute to Mapping specifications
• Utilize SAS/R programming/Python programming skills for clinical trial study submissions
• Develop programs identifying data issues and reporting them to the appropriate team
• Utilize appropriate guidelines to build CDISC/regulatory compliant datasets
• Understand CRF annotations and check for consistency with raw data
• Ability to debug custom functions/SAS Macros and fix issues
• Good understanding of clinical data and domain
• Follow Client Processes and SOPs
• Assist senior team members in quality control processes
• Assist senior team members with team metrics
• Communicate with an internal team to create deliverables for pharmaceutical and CRO clients
• Work in tandem with Biostatistics and Data Management members on clinical projects
• Communicate with programming and statistics leads
• Make sure you are compliant with company policies/SOPs.