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0-2 years
Not Disclosed
10 Sept. 24, 2025
Job Description
Job Type: Full Time Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Job Title:

SAS I

Company: Syneos Health®
Location: USA-NC-Morrisville (Hybrid)
Job ID: 25101856
Updated: September 22, 2025


About Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions organization that accelerates customer success. Our Clinical Development model centers on patients and customers, continuously streamlining processes to improve efficiency and outcomes.

Key Highlights:

  • 29,000 employees across 110 countries

  • Supported 94% of Novel FDA Approved Drugs, 95% of EMA Authorized Products

  • Contributed to 200+ studies across 73,000 sites and 675,000+ trial patients

Culture & Values:

  • Total Self culture – encouraging authenticity and inclusivity

  • Career development, training, recognition, and total rewards

  • Collaborative, innovative, and supportive environment


Job Summary

The SAS I role is an entry-level/early-career position responsible for supporting statistical programming activities using SAS and related tools. This position contributes to the development, validation, and documentation of programs and datasets to support clinical trials and regulatory submissions.


Core Responsibilities

  • Develop, validate, and maintain SAS programs in support of clinical trials.

  • Assist in the creation of analysis datasets, tables, listings, and figures (TLFs).

  • Support data cleaning, data management, and quality checks.

  • Generate documentation in compliance with internal standards and regulatory requirements.

  • Collaborate with biostatisticians, data managers, and project teams to ensure timely delivery of programming tasks.

  • Contribute to process improvement and adherence to standard operating procedures (SOPs).


Qualifications

  • Bachelor’s degree in a relevant field (e.g., Statistics, Life Sciences, Pharmacy) or equivalent experience.

  • Entry-level or early career experience in SAS programming is preferred.

  • Basic understanding of clinical trials, data structures, and regulatory requirements.

  • Strong analytical and problem-solving skills.

  • Effective communication and teamwork abilities.

Technical Skills:

  • Proficiency in SAS and/or related statistical programming languages.

  • Familiarity with Microsoft Office Suite.

  • Exposure to clinical trial datasets and regulatory reporting is a plus.


Benefits & Compensation

  • Company car or car allowance (if applicable)

  • Health benefits: Medical, Dental, Vision

  • 401(k) plan with company match

  • Employee Stock Purchase Plan eligibility

  • Commissions/bonus opportunities based on performance

  • Flexible PTO and sick time (subject to local regulations)

Salary:

  • Base salary depends on qualifications, skills, and experience.


Additional Information

  • Tasks and responsibilities may evolve based on business needs.

  • Equivalent experience, skills, and education may be considered.

  • Syneos Health is committed to diversity, equity, inclusion, and compliance with the Americans with Disabilities Act (ADA).


How to Apply

Join the Syneos Health Talent Network to be considered for this role:
Syneos Health Careers