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Senior Clinical Programmer (Dm Sas)

5+ years
Not Disclosed
10 Oct. 4, 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

🧑‍💻 Position Title:

Senior Clinical Programmer (DM SAS)


🌍 Location:

IND-Hyderabad (Hybrid)


🆔 Job ID:

25102111


🎯 Job Overview:

Serve as lead Clinical Programmer, managing and supporting project deliverables and timelines. Design, write, validate, and maintain software to meet specifications. Act as a first-level Subject Matter Expert (SME), supporting Electronic Data Capture (EDC), reporting, and data processing tools. Lead multiple clinical programming projects, ensure high-quality deliverables, and provide technical guidance to project teams.


🌟 Key Responsibilities:

🔹 Programming & Technical Execution

  • Utilize primary development tools: Medidata, Rave, Oracle OC/RDC, Oracle Inform, SAS, and other supporting tools.

  • Design, write, validate, and maintain software according to specifications and standard procedures.

  • Generate and maintain documentation: specifications, programs, validation efforts, annotated CRFs, database creation, coding setup, edit checks, import/export processing, listings, and custom reports.

  • Monitor applications for workflow alerts, system errors, and performance issues; provide second-tier support.

  • Perform system integration activities, application updates, and user acceptance testing.

🔹 Project & Team Leadership

  • Lead clinical programming activities on 3–10 concurrent studies based on scope and resources.

  • Coordinate and lead development activities within project teams; attend meetings and provide feedback.

  • Provide guidance, training, and support to department members.

  • Collaborate with clients, peers, lead programmers, and project teams to finalize specifications.

  • Review study budgets, monitor scope, manage change orders, and communicate issues impacting project timelines or deliverables.

🔹 Quality & Compliance

  • Ensure high-quality deliverables through senior review of study-level and multi-study programs.

  • Assist with sponsor audits and in-progress audits.

  • Maintain broad knowledge of clinical programming, clinical data management, and industry standards.


🎓 Qualifications & Requirements:

  • Bachelor’s degree preferred, or equivalent combination of education and experience.

  • Minimum 5+ years of experience in Clinical Programming.

  • Experience in listings programming, macro creation, study build, and SAS mapping preferred.

  • Experience in CDSIC Data Mapping, External/Vendor Data Mapping, and DIA preferred.

  • Strong communication and interpersonal skills.

  • Base and Advanced SAS certification preferred.

  • Experience in any therapeutic area is acceptable.

  • Ability to work effectively with sponsors and internal teams.

  • Experience in a matrix-structured environment preferred.

  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Email).

  • Knowledge of programming languages such as PL/SQL, SAS, C#, or VB preferred.

  • Ability to travel up to 25% as required.


Work Environment & Physical Requirements:

  • Hybrid work setup with office/remote-based work.

  • Frequent stationary work and repetitive hand movements.

  • Occasional crouching, bending, and twisting.

  • Light to moderate lifting (up to 15–20 lbs).

  • Regular and consistent attendance; ability to manage multiple priorities in a dynamic environment.


🌐 Why Syneos Health:

  • Work with a leading integrated biopharmaceutical solutions organization across 110 countries.

  • Professional growth, training, and mentorship opportunities.

  • Supportive, inclusive Total Self culture emphasizing diversity and belonging.

  • Exposure to high-impact projects involving FDA-approved drugs, EMA-authorized products, and major clinical trials.


📌 Summary:

Lead clinical programming projects, provide technical expertise and mentorship, manage multiple studies, ensure high-quality data deliverables, and support clinical programming teams and sponsor needs.