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Clinical Programmer Iii (India)

2-5 years
₹10 – ₹14 LPA
10 July 31, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Clinical Programmer III – SAS & EDC (India)
Location: Bengaluru or Chennai, Karnataka/Tamil Nadu (Hybrid)
Department: Clinical Trial Organization (CTO)
Position Type: Full-Time
Experience Required: 2–5 Years
Openings: 1


Job Overview:
Allucent is seeking a Clinical Programmer III with strong SAS and EDC programming experience to join our global data operations team. You will play a crucial role in building and maintaining clinical databases, supporting regulatory-compliant data programming, and contributing to the accuracy, quality, and integrity of clinical trial data across various therapeutic areas.


Key Responsibilities:

  • Design, build, test, and release clinical databases, ensuring adherence to study protocols and regulatory standards.

  • Develop and validate SAS programs for metric reporting, data review listings, and data exchange activities.

  • Apply CDISC standards (CDASH, TAUGs, SDTM) during database creation and data warehousing processes.

  • Review eCRF completion guidelines and support UAT activities.

  • Collaborate with cross-functional teams to resolve programming and data specification queries.

  • Participate in sponsor/study meetings and provide technical guidance on database architecture and validation.

  • Maintain updated knowledge of evolving data management technologies and programming best practices.

  • Train department staff on clinical programming tools and quality practices.

  • Contribute as a Subject Matter Expert (SME) in internal audits, process improvements, and SOP enhancements.


Required Qualifications:

  • Bachelor's or Master's degree in Life Sciences, Computer Science, or related technical field.

  • 2–5 years of clinical programming experience in a CRO, pharmaceutical, or biotech setting.

  • Strong SAS programming skills and experience with EDC systems.

  • Good understanding of ICH-GCP(R2), GDPR/HIPAA, and local/global regulatory requirements.

  • Knowledge of CDISC standards (CDASH, TAUGs, SDTM).

  • Proficiency in PL/SQL and clinical data management tools.

  • Strong analytical mindset, problem-solving ability, and communication skills.

  • Ability to work collaboratively in a dynamic, fast-paced environment.


Preferred Traits:

  • Solution-focused approach with a positive, team-driven attitude.

  • Openness to mentoring and continuous learning.

  • Eagerness to propose and implement efficiency-improving initiatives.


Benefits:

  • Competitive salary with performance-linked variable pay

  • Comprehensive health and retirement benefits

  • Departmental training and development budget

  • Flexible hybrid work model (2–3 days office-based)

  • Buddy program, mentoring, and leadership opportunities

  • Access to GoodHabitz training platform

  • Spot Bonus and Loyalty Award programs

  • Internal career growth opportunities


Estimated Salary: ₹10 – ₹14 LPA (depending on skills and experience)