🧑💻 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.
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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Auckland |New Zealand :
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Kyiv |Lima Region :
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