Novotech, a leading global clinical research organization (CRO), is expanding its India team. The company is hiring talented professionals for two full-time roles — Statistical Programmer II and Investigator Grant Specialist (Clinical Document Specialist) — at its Bangalore office.
These positions offer a unique opportunity to work in a dynamic, data-driven environment, supporting global clinical trials and advancing life-changing biotech innovations.
💻 1. Statistical Programmer II
Location:
Helios Business Park, Bangalore, India
About the Role:
The Statistical Programmer II is responsible for SAS programming, dataset development, and statistical deliverables for clinical studies. The role involves close collaboration with biostatisticians, data management, and project teams to ensure regulatory compliance and data integrity.
Key Responsibilities:
- Review clinical study protocols and programming requirements.
- Develop and validate SDTM and ADaM datasets per CDISC standards.
- Generate tables, listings, and figures (TFLs) using SAS.
- Conduct peer reviews and mentor junior programmers.
- Ensure adherence to GCP, ICH, and company SOPs.
- Participate in department meetings and programming standard updates.
Qualifications:
- Master’s degree in Life Sciences, Computer Science, Statistics, or related field with 1 year of experience, or
Bachelor’s degree with 2 years of SAS programming experience in a CRO/pharma setting. - Strong SAS skills and knowledge of CDISC standards.
- Ability to work independently on technical deliverables.
Benefits:
- Flexible working hours & hybrid options.
- Paid parental leave for both parents.
- Professional development & mentorship programs.
- Inclusive culture supporting diversity (LGBTQ+, disability-friendly).
📁 2. Investigator Grant Specialist (Clinical Document Specialist)
Location:
Helios Business Park, Bangalore, India
About the Role:
The Investigator Grant Specialist, also known as a Clinical Document Specialist (CDS), supports the management and quality control of Trial Master Files (TMF) for clinical trials. The role ensures that essential study documentation meets ICH-GCP and Novotech/Client SOP standards.
Key Responsibilities:
- Set up, maintain, and QC electronic & paper TMFs.
- Ensure compliance with ICH GCP, local/global regulations, and company SOPs.
- Manage essential clinical trial documents and submission readiness.
- Support inspection preparation and document archiving.
Qualifications:
- Bachelor’s degree in Life Sciences or related field.
- Prior TMF or clinical document management experience preferred.
- Strong understanding of clinical research processes and regulatory requirements.
Benefits:
- Global exposure in a top-tier CRO.
- Collaborative and growth-oriented culture.
- Wellness and learning initiatives for career advancement.
🚀 Why Join Novotech
Novotech is recognized for its ISO 9001 and ISO 27001 certifications, reflecting its commitment to quality and data security. With 34 offices worldwide and 3000+ employees, Novotech offers exposure to multinational studies, diverse therapeutic areas, and global career mobility.
📝 Application Instructions
Application Link for Statistical Programmer II
Application Link for Investigator Grant Specialist
