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Principal Stat Programmer

0-2 years
Not Disclosed
10 Jan. 31, 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

πŸ“Œ Principal Statistical Programmer | Syneos Health
πŸ“ Location: India (Home-Based)
πŸš€ Leading Biopharmaceutical Solutions Organization

🌟 About Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions organization. We are driven by the goal of accelerating customer success by translating clinical, medical affairs, and commercial insights into outcomes that address the challenges of modern market realities.

πŸ“ About the Role

The Principal Statistical Programmer will be responsible for developing custom programming code to generate summary tables, data listings, graphs, and derived datasets, ensuring high-quality outputs. The role requires leading statistical programming activities, mentoring team members, and participating in regulatory submissions using CDISC Standards. You will be accountable for the on-time delivery of multiple concurrent projects.

πŸ” Key Responsibilities

Programming & Project Management

βœ” Develop Custom Code: Utilize SAS or other required software to develop programming code, ensuring compliance with statistical analysis plans and programming specifications.
βœ” Program Validation: Perform validation programming and resolve discrepancies alongside other project team members.
βœ” Manage Project Timelines: Track and adjust timelines across multiple projects, ensuring efficient workload management and timely delivery of outputs.
βœ” Lead Programming Teams: Supervise the programming activities of other team members, ensuring progress is aligned with project goals.

Mentoring & Collaboration

βœ” Mentorship: Guide and train programming personnel by developing courses, reviewing work, and providing feedback.
βœ” Collaborate Across Teams: Work closely with biostatisticians, CDISC experts, and other team members to ensure programming standards are met and that documentation is aligned with regulatory guidelines.

Compliance & Tools Development

βœ” Regulatory Compliance: Serve as an expert in CDISC Standards and assist in submissions to regulatory agencies.
βœ” Programming Tools Development: Contribute to the development of programming tools and macros to standardize processes and improve efficiency.

πŸ“‹ Qualifications

πŸŽ“ Degree: Undergraduate degree in a scientific or statistical discipline (or equivalent programming experience).
πŸ“Œ Experience: Extensive programming experience with SAS in clinical trials, including leadership of complex, global projects.
πŸ“Œ Expertise: Knowledge of CDISC Standards for regulatory submissions and mentoring experience.
πŸ“Œ Skills: Excellent written and verbal communication skills, particularly in English.

🌍 Why Syneos Health?

🌟 Career Development: Syneos Health is committed to supporting your growth through training, mentorship, and peer recognition.
🌍 Inclusive Culture: We foster a workplace that values diverse perspectives and where everyone feels like they belong.
πŸ’Ό Impact: Syneos Health has worked on 94% of FDA-approved drugs in the last 5 years.

πŸ“© Apply Now