📢 For Latest Job Updates
📲 Join WhatsApp Channel
💼 Follow on LinkedIn
✔ Verified by Medical Jobs India
Hiring Associate Clinical Data Scientist
🏢 Novartis
📍 Hyderabad
⏳ 0–4 Years
💰 ₹4 – ₹8 LPA
Looking to build your career in clinical data management & data science? Novartis is hiring an Associate Clinical Data Scientist in Hyderabad. This role offers hands-on exposure to clinical trials, data validation, and global pharma projects.
📋 Job Overview
- Role: Associate Clinical Data Scientist
- Location: Hyderabad (Office-based)
- Experience: 0–4 Years
- Department: Clinical Data Management
- Company: Novartis
📌 Key Responsibilities
- Clinical data collection & validation
- Database management & delivery
- Support CSP, DHP & DRP development
- Perform UAT & data review
- Handle coding & validation checks
- Ensure GCP compliance
- Support audits & QC activities
🎓 Eligibility
- B.Pharm / M.Pharm / PharmD / BSc / MSc / Life Sciences
- 0–4 years experience
- Basic knowledge of clinical trials preferred
💻 Required Skills
- Clinical Data Management basics
- Data validation & databases
- Attention to detail
- Communication & teamwork
🚀 Career Growth
- Clinical Data Scientist
- Clinical Data Manager
- Clinical SAS Programmer
- Clinical Data vs SAS Guide
💡 Interview Tips
- Revise CDM & SDTM basics
- Understand clinical trial workflow
- Practice Quiz
📄 Resume Tips
- Add clinical projects or internships
- Highlight data & validation skills
- Use keywords: CDM, SDTM, Data Review
- CDISC Guide
📌 Tip: High-demand role in Clinical Data Science — apply early.
🚀 Job Application Link
📌 Important Note Before You Apply:
Kindly read the full job description carefully before applying. Ensure your profile aligns with clinical data management, data review and cleaning strategies, data validation specifications, listing reviews, and global clinical trial compliance standards before proceeding.
Kindly read the full job description carefully before applying. Ensure your profile aligns with clinical data management, data review and cleaning strategies, data validation specifications, listing reviews, and global clinical trial compliance standards before proceeding.
