Sr Statistical Programmer(ADaM & TLF)

Syneos Health; Hyderabad; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

Syneos Health in Hyderabad is seeking an experienced Statistical Programmer to develop SAS code for SAP-driven tables, listings, and graphs. You will validate outputs, maintain documentation, and collaborate with biostatisticians and project teams to ensure regulatory compliance.

The role requires 5+ years in SAS programming within a clinical trial setting, with strong CDISC-ADAM/TLF expertise and excellent communication skills in English.

Qualifications

• Undergraduate degree in a scientific or statistical discipline or equivalent experience.
• 5+ years of experience in SAS programming, preferably in a clinical trial environment.
• Strong experience in CDISC-ADAM and TLF generation; Base SAS and SAS Macros.
• Excellent written and verbal communication; English proficiency.

Responsibilities

• Develop custom programming code to generate tables, listings, graphs per SAP and specs.
• Ensure outputs meet quality standards; perform validation and resolve discrepancies with team.
• Maintain organized project documentation, testing, and QC documents for inspections.
• Lead programming activities, estimate timelines, and coordinate with sponsors and team.

Skills

Excellent communication

English proficiency

Education

Undergraduate degree in science or statistics

Tools

SAS Programming

Base SAS

SAS Macros

CDISC-ADAM & TLF generation

Job description

Role & responsibilities

Job Responsibilities

• Uses SAS or other software to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications.
• Works to ensure that outputs meet quality standards and project requirements. Performs validation programming and works with other Programmers, Biostatisticians, and other project team members to resolve discrepancies or any findings. Keeps project team members informed of programming progress and issues requiring their attention. Follow applicable SOPs, WIs, and relevant regulatory guidelines (e.g. ICH).
• Maintains well organized, complete, and up-to-date project documentation, testing, and verification/quality control documents and programs ensuring inspection readiness.
• Manages scheduling and time constraints across multiple projects at a time, sets goals based on priorities from management, and adapts to timeline or priority changes by reorganizing daily workload. Develops specifications for datasets and outputs of any complexity according to statistical and sponsor requirements. Anticipates and addresses potential programming issues, reflects forethought, establishes the basis for efficient programming and accurately defines all variables to be accepted by peer review and sponsor/requestor with little rework.
• Prepares in advance for internal meetings, contributes ideas, and demonstrates respect for opinions of others.
• Conducts effective internal meetings (appropriate in format, frequency and attendance). Distributes relevant information in advance. Ensures minutes are promptly and accurately distributed. Follows action items through to completion, and maintains order and focus of meetings, working toward consensus. Displays willingness to work with others and assist with projects and initiatives as necessary to meet the needs of the business. Negotiates and establishes accurate time estimates for completion of study programming activities with internal team members and statistical programming management, and completes project programming activities within timeframe allotted.
• Acts as the lead statistical programmer. Directs the programming activities of other programming personnel and monitors progress on programming deliverables. Reviews project documentation such as Statistical Analysis Plan, mock shells, programming specifications, annotated CRFs, and SAS database design. Provides feedback to the appropriate project team members which reflects forethought and reduces inefficiencies in programming activities.
• Participates in sponsor meetings, kickoff meetings, and bid defense meetings as statistical programming representative, as required by sponsor. Contributes to the mentoring of programming personnel through developing training courses, presenting training materials, reviewing work, and providing feedback or guiding new associates in process. Transfers deliverables. Performs other work-related duties as assigned.
• Minimal travel may be required.

Qualifications:

• Undergraduate degree, preferably in a scientific or statistical discipline; in lieu of degree, an equivalent combination of education and demonstrated programming experience.
• Require 5+ years of experience in SAS Programming or other required software, preferably in a clinical trial environment.
• Must have strong experience in CDISC- ADAM & TLF generation.
• Good to have experience of submission activities.
• Must have strong experience in Base SAS, Advance SAS/ SAS Macros.
• Excellent written and verbal communication skills.
• Ability to read, write, speak and understand English.