Senior Statistical Programmer

🔥 1 hour ago

🇮🇳 India – Remote

⏰ Full Time

🟠 Senior

🖥 Software Engineer

👻 Ghost score 10%

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Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Use SAS or other software to develop custom programming code for summary tables, data listings, graphs, and derived datasets • Ensure outputs meet quality standards and project requirements • Perform validation programming and resolve discrepancies with Programmers, Biostatisticians, and project team members • Maintain complete, current project documentation, testing, and quality control materials for inspection readiness • Manage scheduling and time constraints across multiple projects • Develop specifications for datasets and outputs according to statistical and sponsor requirements • Prepare for and conduct internal meetings, distribute information and minutes, and follow action items through completion • Estimate and complete study programming activities within allotted timelines • Act as lead statistical programmer and direct programming activities of other personnel • Review Statistical Analysis Plans, mock shells, programming specifications, annotated CRFs, and SAS database designs • Participate in sponsor, kickoff, and bid defense meetings as the statistical programming representative • Mentor programming personnel through training, work review, feedback, and guidance • Transfer deliverables and perform other assigned work-related duties

🎯 Requirements

• Undergraduate degree, preferably in a scientific or statistical discipline; in lieu of degree, an equivalent combination of education and demonstrated programming experience • Extensive programming experience in SAS or other required software, preferably in a clinical trial environment • Excellent written and verbal communication skills • Ability to read, write, speak and understand English • Ability to develop custom programming code for clinical trial outputs • Knowledge of statistical analysis plans, programming specifications, annotated CRFs, and SAS database design • Knowledge of applicable SOPs, work instructions, and relevant regulatory guidelines such as ICH • Ability to lead statistical programming activities and direct other programming personnel • Ability to manage multiple projects, schedules, priorities, and timelines • Ability to participate in sponsor, kickoff, and bid defense meetings • Ability to mentor programming personnel and provide feedback

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Inclusive culture • Minimal travel may be required