Sr Statistical Programmer - ADAM & TLFs

Syneos Health; United States; Remote; USD 80,000 - 100,000; Full time

Job summary

An established industry player is seeking a skilled Statistical Programmer to join their dynamic team. This role involves developing custom programming code to generate critical datasets and ensuring quality outputs in compliance with regulatory standards. With a focus on collaboration, the ideal candidate will lead programming activities, mentor junior staff, and contribute to internal meetings, all while managing multiple projects efficiently. If you have a strong background in SAS or R programming and thrive in a clinical trial environment, this opportunity offers a chance to make a significant impact in a forward-thinking organization.

Qualifications

• 5+ years of programming experience in SAS or R in a clinical trial environment.
• Hands-on experience with ADaM & TLFs Safety & Efficacy using CDISC standards.

Responsibilities

• Develop custom programming code to generate summary tables and datasets.
• Ensure outputs meet quality standards and project requirements.
• Lead programming activities and mentor programming personnel.

Skills

SAS Programming

R Programming

Clinical Trial Standards (CDISC)

Communication Skills

Job description

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.
• Follows 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, 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 the 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.

What We're Looking For
• Should have at least 5 years of hands-on experience with ADaM & TLFs Safety & Efficacy using CDISC standards.
• Should have at least 5 years of extensive programming experience in SAS or R with expertise in a clinical trial environment.
• Excellent written and verbal communication skills.
• Ability to read, write, speak, and understand English.