Centralized Monitoring Analyst (Level I & II)
Thermo Fisher Scientific is hiring Centralized Monitoring Analysts (Level I & II) in Bangalore. This opportunity is ideal for professionals with experience in Clinical Research, Clinical Monitoring, Clinical Data Management (CDM), Biostatistics, and Clinical Trial Analytics.
The role focuses on risk-based monitoring, clinical data review, trend analysis, signal detection, and centralized monitoring activities supporting global clinical trials.
📋 Job Overview
| Particulars | Details |
|---|---|
| Company | Thermo Fisher Scientific |
| Position | Centralized Monitoring Analyst (Level I & II) |
| Location | Bangalore |
| Work Mode | Hybrid |
| Experience | 2+ Years |
| Employment Type | Full-Time |
| Industry | Clinical Research & Pharmaceutical Services |
💼 Key Responsibilities
- Review Clinical Trial Data Using Analytics Platforms.
- Perform Centralized Monitoring Activities.
- Identify Potential Risks, Trends, and Signals.
- Support Risk-Based Monitoring Programs.
- Generate Monitoring Reports and Documentation.
- Track Operational and Patient-Level Data Issues.
- Communicate Findings to Clinical Project Teams.
- Support Review Setup and Database Activities.
- Ensure Compliance with SOPs and Monitoring Plans.
- Assist in Data Quality and Risk Management Activities.
🎓 Eligibility Criteria
Educational Qualification
- B.Pharm
- M.Pharm
- Life Sciences
- Biotechnology
- Clinical Research
- Nursing
- Medicine
- Statistics / Biostatistics
- Related Healthcare Disciplines
Experience Required
- Minimum 2 Years Relevant Experience Preferred.
- Clinical Monitoring Experience.
- Clinical Data Management (CDM).
- Clinical Trial Operations.
- Biostatistics or Clinical Analytics Experience.
🧠 Required Skills
- Risk-Based Monitoring (RBM)
- Clinical Trial Analytics
- Clinical Data Review
- Medical Terminology
- Problem Solving Skills
- Microsoft Excel & PowerPoint
- Clinical Documentation
- Data Trend Analysis
- Communication Skills
- Attention to Detail
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💰 Salary & Benefits
Based on industry benchmarks for Centralized Monitoring and Clinical Analytics professionals:
Estimated Salary: ₹6 LPA – ₹12 LPA
Actual compensation may vary depending on experience, qualifications, and company policies.
Employee Benefits
- Hybrid Work Model
- Global Clinical Trial Exposure
- Professional Development Programs
- International Team Collaboration
- Health & Wellness Benefits
- Learning and Certification Support
- Career Advancement Opportunities
- Performance-Based Rewards
🌟 Why Join Thermo Fisher Scientific?
- Work on Global Clinical Trials Across Multiple Therapeutic Areas.
- Exposure to Advanced Trial Data Analytics.
- Learn Risk-Based Monitoring Methodologies.
- Collaborate with Leading Pharmaceutical Companies.
- Strong Learning and Development Culture.
- Build Expertise in Clinical Operations and Analytics.
- Excellent Career Growth Opportunities.
- Work with One of the World's Leading CRO Organizations.
📈 Career Growth Opportunities
- Senior Centralized Monitoring Analyst
- Clinical Data Analyst
- Risk-Based Monitoring Specialist
- Clinical Operations Associate
- Clinical Data Management Specialist
- Clinical Trial Analytics Lead
- Clinical Operations Manager
- RBM Program Lead
📑 Resume Tips for Centralized Monitoring Roles
- Highlight Clinical Trial Experience.
- Mention RBM and Monitoring Activities.
- Include Clinical Data Review Experience.
- Showcase CDM or Clinical Operations Exposure.
- Mention Trend Analysis and Risk Identification Activities.
- Keep Resume ATS-Friendly and Results Focused.
Before applying, read:
Healthcare & Pharma Job Application Guide🎯 Interview Tips for Centralized Monitoring Analyst
Candidates preparing for the Thermo Fisher Scientific interview should focus on:
- Risk-Based Monitoring (RBM) Concepts.
- Centralized Monitoring Process.
- Clinical Trial Phases and Terminology.
- Clinical Data Review Techniques.
- Protocol Deviations and Risk Indicators.
- ICH-GCP Guidelines.
- Clinical Data Management Basics.
- Medical Terminology.
- Data Trend Analysis.
- HR and Behavioral Questions.
Practice using:
Clinical Research Knowledge Hub📌 How to Apply?
Interested candidates should prepare an updated resume highlighting clinical research experience, monitoring activities, clinical data review expertise, and risk management knowledge.
Before applying, read:
Healthcare & Pharma Job Application Guide🚀 Apply Now
Interested and eligible candidates can apply through the official Thermo Fisher Scientific Careers portal.
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❓ Frequently Asked Questions
Q. Who can apply for this role?
Candidates from Pharmacy, Life Sciences, Biotechnology, Clinical Research, Nursing, Medicine, Statistics, and related healthcare disciplines.
Q. Is prior experience required?
Yes. Candidates with around 2 years of experience in Clinical Monitoring, CDM, Biostatistics, or Clinical Operations are preferred.
Q. What is the expected salary?
Approximately ₹6–12 LPA depending on experience and company policies.
Q. What are the major responsibilities?
Centralized monitoring, risk identification, clinical data review, trend analysis, and clinical trial analytics.
Q. Is this role suitable for Clinical Research Associates (CRAs)?
Yes. CRA, CDM, Clinical Operations, and Clinical Analytics professionals can find this role highly relevant.
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