Sr Statistical Programmer

2+ years

Not Disclosed

India

10 March 24, 2025

Job Description

Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Sr Statistical Programmer -

Updated: March 20, 2025
Location: India-Asia Pacific - IND-Home-Based
Job ID: 25002032

Description

Senior Statistical Programmer

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything we do. We continuously look for ways to simplify and streamline our work to not only make Syneos Health easier to work with but also make it easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies because we are passionate about changing lives.

Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE

Why Syneos Health:

Passionate about developing people through career progression, supportive line management, technical training, and a peer recognition program.
Committed to a Total Self culture – allowing you to be authentic.
Dedicated to creating an environment where diversity of thoughts, backgrounds, and perspectives makes everyone feel they belong.

Job Responsibilities:

Use 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.
Ensure that outputs meet quality standards and project requirements.
Perform validation programming and work with other Programmers, Biostatisticians, and project team members to resolve discrepancies.
Keep project team members informed of programming progress and issues requiring attention.
Follow applicable SOPs, WIs, and relevant regulatory guidelines (e.g., ICH).
Maintain well-organized, complete, and up-to-date project documentation, ensuring inspection readiness.
Manage scheduling and time constraints across multiple projects, set goals based on management priorities, and adapt to timeline or priority changes.
Develop specifications for datasets and outputs of any complexity according to statistical and sponsor requirements.
Conduct effective internal meetings, distribute relevant information in advance, and ensure action items are completed.
Display willingness to work with others and assist with projects as necessary.
Negotiate and establish accurate time estimates for study programming activities with internal team members and management.
Act as the lead statistical programmer, directing the programming activities of others and monitoring progress on deliverables.
Review project documentation such as Statistical Analysis Plan, mock shells, programming specifications, and annotated CRFs.
Participate in sponsor meetings, kickoff meetings, and bid defense meetings as a statistical programming representative.
Mentor programming personnel by developing training courses, presenting materials, and reviewing work.
Transfer deliverables as required.
Perform 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.
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.

Get to Know Syneos Health:

Over the past 5 years, we have worked with:

94% of all Novel FDA Approved Drugs
95% of EMA Authorized Products
Over 200 Studies across 73,000 Sites and 675,000+ Trial patients

No matter what your role is, you’ll take the initiative and challenge the status quo in a highly competitive and ever-changing environment.

Learn more about Syneos Health.

Additional Information:

Tasks, duties, and responsibilities listed in this job description are not exhaustive. The company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered. Nothing contained herein should be construed to create an employment contract. The company is committed to compliance with the Americans with Disabilities Act, including providing reasonable accommodations when appropriate to assist employees or applicants in performing essential job functions.

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