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Hiring Clinical Data Manager & Clinical Lead Analyst
🏢 Novotech (Global CRO)
📍 Bangalore
🎓 Life Sciences / Pharma
⏳ 5–10 Years
Novotech is hiring experienced professionals for Clinical Data Manager (CDM) and Clinical Lead Analyst roles. Excellent opportunity for candidates looking to grow in clinical data management, CRO operations, and clinical analytics.
👉 Learn before applying: Clinical Data vs SAS Career Guide
📊 Clinical Data Manager (CDM)
Job Overview:
Responsible for end-to-end clinical trial data management ensuring accuracy, compliance, and timely delivery of high-quality clinical datasets.
- Location: Bangalore (Helios Business Park)
- Experience: 6–10 Years
- Qualification: Life Sciences / Pharmacy / Clinical / Medical
- Domain: Clinical Data Management (CDM)
Key Responsibilities:
- Develop Data Management Plans (DMP)
- Database design, edit checks & validation
- Clinical data cleaning & reconciliation
- Manage EDC systems and clinical databases
- Ensure compliance with GCDMP & SOPs
- Coordinate with sponsors and CRO teams
- Train and supervise junior team members
- Project budgeting and financial tracking
Required Skills:
- Strong knowledge of GCDMP & CDISC
- Hands-on EDC tools (Medidata, Oracle, etc.)
- Clinical trial lifecycle understanding
Salary (Estimated): ₹10 – ₹25 LPA
📈 Clinical Lead Analyst (CLA)
Job Overview:
Supports clinical trial execution through data-driven insights, performance monitoring, and risk management.
- Location: Bangalore
- Experience: 5+ Years (3+ Years Clinical Ops/Analytics)
- Qualification: Life Sciences / Pharmacy
- Domain: Clinical Analytics / Operations
Key Responsibilities:
- Monitor clinical KPIs & performance metrics
- Analyze risks and protocol deviations
- Prepare dashboards & reports
- Work on CTMS, EDC, IWRS systems
- Support CAPA and compliance processes
- Coordinate with clinical teams
Required Skills:
- Strong Excel & data analysis
- Knowledge of ICH-GCP guidelines
- Clinical operations experience
Salary (Estimated): ₹8 – ₹18 LPA
🌍 Why Join Novotech?
- Global CRO exposure (30+ countries)
- Work on international clinical trials
- Strong career growth opportunities
- Learning & mentorship programs
- Flexible and inclusive work culture
💡 Interview Tips
- Revise GCDMP, ICH-GCP guidelines
- Prepare EDC & database questions
- Understand clinical trial lifecycle
- Practice scenario-based questions
👉 Practice now: Clinical Quiz
📄 Resume Tips
- Mention EDC tools & CDISC clearly
- Highlight clinical trial experience
- Use keywords: GCP, CDM, CTMS
- Show project-level contributions
❓ Frequently Asked Questions
- Freshers eligible? ❌ No (Experienced roles)
- Best role? CDM for leadership, CLA for analytics
- CRO experience required? Preferred
🚀 Job Application Links
📌 Important Note Before You Apply:
Kindly read the full job description carefully for your selected role before applying. Ensure your profile aligns with clinical data management (CDM) standards, data validation, protocol review, or clinical data analysis requirements before submitting your details.
Kindly read the full job description carefully for your selected role before applying. Ensure your profile aligns with clinical data management (CDM) standards, data validation, protocol review, or clinical data analysis requirements before submitting your details.
📥 How to Apply
- Read the full job description thoroughly for your desired role
- Click on the specific Apply Now button above
- Fill out the application form on the official portal carefully
- Upload your updated resume or CV
- Submit your application
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