Syneos Health® is a leading fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. With a focus on clinical, medical affairs, and commercial insights, we drive meaningful outcomes to address modern market challenges.
As a Statistical Programmer I, you will play a crucial role in clinical trial data analysis by using SAS or other statistical software to generate summary tables, data listings, graphs, and derived datasets. You will ensure outputs meet quality standards and regulatory requirements while collaborating with Biostatisticians and project teams.
Key Responsibilities:
✔ Use SAS/R to create statistical outputs as per the Statistical Analysis Plan (SAP).
✔ Perform validation programming and resolve discrepancies with the team.
✔ Maintain well-organized project documentation for compliance and inspection readiness.
✔ Manage multiple projects, adapt to timeline changes, and prioritize tasks efficiently.
✔ Follow SOPs, WIs, and ICH guidelines to ensure regulatory compliance.
✔ Collaborate with cross-functional teams and contribute to process improvements.
✔ Minimal travel may be required.
Qualifications & Skills:
✅ Undergraduate degree in a scientific/statistical discipline (2024/2025 pass-outs preferred).
✅ Basic knowledge of R programming and proficiency in SAS (experience in clinical trials is a plus).
✅ Strong analytical and problem-solving skills.
✅ Excellent written and verbal communication in English.
✅ Ability to work in a fast-paced, remote team environment.
Why Join Syneos Health?
✔ Global Impact: Work with 94% of Novel FDA-Approved Drugs and 95% of EMA-Authorized Products.
✔ Career Growth: Continuous training, mentorship, and progression opportunities.
✔ Inclusive Culture: A “Total Self” environment where diversity and authenticity are celebrated.
✔ Innovative Projects: Contribute to 675,000+ clinical trial patients across 73,000 sites.
