Clinical SAS Programmer – India
Location: Remote – India
Employment Type: Permanent, Full-time
Professional Level: Mid-Level
About the Role
Indero, a global clinical research leader in dermatology and rheumatology, is seeking an experienced Clinical SAS Programmer to lead programming activities for clinical trials. This role focuses on SAS Data Listings for Data Review, Safety Review, Centralized Monitoring, and Reporting, ensuring high-quality deliverables within agreed timelines.
The Clinical SAS Programmer will collaborate across departments to optimize data workflows, develop productivity strategies, and maintain compliance with regulatory standards, sponsor requirements, and Indero SOPs.
Key Responsibilities
Develop and maintain SAS Data Review Listings based on protocol, EDC database, and data validation specifications.
Create a centralized library of SAS Data Review Listings for clinical trial use.
Generate Safety Review Listings and reports to support Centralized Monitoring initiatives.
Document SAS code changes, programs, and specifications for audit readiness and traceability.
Assist in the development and maintenance of SOPs related to clinical data standards.
Collaborate with cross-functional teams to improve productivity, data quality, and reduce cycle times.
Ensure compliance with applicable regulatory requirements, FDA, Health Canada, and industry guidelines.
Required Qualifications
Education:
Bachelor of Science in Computer Science, Statistics, Life Sciences, Engineering, or related field required.
Master’s degree is a plus.
Experience:
3–5 years of clinical research experience in biotechnology, pharmaceuticals, or CROs.
Minimum 3 years of SAS programming experience in clinical trials.
Experience with clinical trial data, EDC databases, and data validation.
Skills:
SAS certification or advanced programmer expertise is an asset.
Strong knowledge of regulatory requirements and the drug development process.
Highly organized with excellent project planning, time management, and attention to detail.
Strong verbal and written communication skills in English.
Ability to manage multiple priorities in a fast-paced, deadline-driven environment.
Knowledge of Good Clinical Practices (GCP) and regulatory guidelines (FDA, Health Canada).
Work Environment and Benefits
Fully remote work position in India; occasional meetings may be scheduled outside regular hours.
Flexible work schedule with full-time permanent employment.
Ongoing learning and development opportunities within a global CRO environment.
Collaborative, innovation-driven workplace culture with exposure to global clinical trial projects.
About Indero
Indero, formerly Innovaderm, is a global clinical research leader in dermatology and rheumatology, delivering full-service solutions from protocol design and patient recruitment to trial monitoring and biometrics. With over 25 years of experience and a global footprint across North America, Europe, Asia Pacific, and Latin America, Indero provides rigorous scientific and operational expertise to biotech and pharmaceutical sponsors worldwide.
Indero is committed to equity, inclusion, and providing accommodations throughout the recruitment process. Applicants must be legally authorized to work in India.
Apply Now
Advance your career as a Clinical SAS Programmer with Indero. Contribute to global clinical trials, optimize data workflows, and ensure high-quality, regulatory-compliant outputs that support life-changing therapies worldwide.
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