🧑💻 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.
Gujarat :
Ahmedabad | Ankleshwar | Baroda | Bharuch | Gandhinagar | Gujarat | Halol | Jhagadia | Mehsana | Tarasadi | Vadodara | Vapi |Maharashtra :
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Queensland |Melbourne :
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Brazil | Sao paulo |Attica :
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Madrid |Cebu Province :
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Ho Chi Minh City |Italy :
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Japan | Saitama |Tokyo :
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Kyiv |Lima Region :
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