Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Clinical Programmer Iii (India)

Allucent
Allucent
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)