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Senior Clinical Programmer (Dm Sas)

5+ years
Not Disclosed
10 Oct. 4, 2025
Job Description
Job Type: Full Time 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


🆔 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) for clinical programming and data management, supporting Electronic Data Capture (EDC), reporting, and data processing tools. Ensure high-quality, timely deliverables across multiple concurrent clinical studies.


🌟 Key Responsibilities:

🔹 Programming & Technical Execution

  • Utilize 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, including specifications, programs, validation efforts, annotated CRFs, database creation, coding configuration, edit-check procedures, import/export setup, listings, and custom reports.

  • Lead clinical programming activities on 3–10 concurrent studies depending on scope and resource requirements.

  • 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

  • Serve on project teams to coordinate and lead clinical programming activities.

  • Attend meetings, provide constructive feedback, and communicate issues impacting project timelines, scope, or budget.

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

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

  • Review study budgets, monitor scope, and manage change orders.

🔹 Quality & Compliance

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

  • Assist with sponsor audits and in-progress audit activities.

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


🎓 Qualifications & Requirements:

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

  • Minimum 5+ years of experience in Clinical Programming.

  • Experience in listings programming, creating macros, study build, and SAS mapping preferred.

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

  • Strong communication and interpersonal skills.

  • SAS certification (base and advanced) preferred.

  • Experience across any therapeutic area is acceptable.

  • Ability to work effectively with sponsors and internal teams at all levels.

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

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

  • Ability to travel up to 25% as needed.


Work Environment & Physical Requirements:

  • Office/remote-based with occasional travel.

  • 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.

  • Opportunities for professional growth, training, and mentorship.

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

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


📌 Summary:

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