Thermo Fisher Scientific has announced new openings for Centralized Monitoring Analyst (Level I & II) positions in Bangalore, India. The company is seeking professionals with experience in clinical monitoring, clinical data management, biostatistics, or related clinical research functions.
This is an excellent opportunity for candidates looking for Centralized Monitoring Analyst jobs in Bangalore, clinical data analytics jobs in India, and clinical research analyst jobs at Thermo Fisher Scientific. The role offers exposure to global clinical trials and advanced data analytics supporting some of the world’s leading pharmaceutical and biotechnology companies.
About Thermo Fisher Scientific
Thermo Fisher Scientific is a global leader in scientific research services, diagnostics, and pharmaceutical development. Over the last five years, the company has supported the world’s top 50 pharmaceutical companies and more than 750 biotechnology organizations across over 2,700 clinical trials in more than 100 countries.
Job Details
- Position: Centralized Monitoring Analyst (Level I & II)
- Department: Clinical Operations / Trial Data Analytics
- Location: Bangalore, Karnataka, India
- Work Mode: Hybrid
- Employment Type: Full-Time
- Work Schedule: Standard (Monday–Friday)
- Experience Required: 2+ years preferred
- Industry: Clinical Research and Pharmaceutical Services
Key Responsibilities
As a Centralized Monitoring Analyst, you will:
- Review clinical trial data using multiple analytics tools and systems.
- Perform data reviews according to centralized monitoring plans.
- Identify, characterize, and track potential risks, signals, and operational issues.
- Document findings according to departmental procedures and global SOPs.
- Support risk characterization and reporting activities.
- Assist in review setup activities, including database updates and report generation.
- Analyze patient and operational trial data to identify trends and emerging issues.
- Communicate potential risks and findings to project teams for corrective actions.
Educational Qualifications
Candidates with the following qualifications may apply:
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Statistics, Biostatistics, Clinical Research, Nursing, Medicine, or related disciplines.
- Equivalent education, training, and directly related experience may also be considered.
Experience Requirements
Preferred candidates should possess:
- Minimum 2 years of relevant experience.
- Experience in:
- Clinical Monitoring
- Clinical Data Management (CDM)
- Biostatistics
- Clinical Trial Operations
- Clinical Data Analytics
- Centralized Monitoring activities
Required Skills
Successful candidates should have:
- Strong analytical and problem-solving abilities
- Excellent numerical aptitude and attention to detail
- Understanding of clinical trial processes and protocols
- Knowledge of centralized monitoring plans and project documentation
- Medical terminology knowledge
- Good communication skills in English
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Ability to maintain confidentiality of clinical and proprietary data
- Prioritization and workload management skills
- Team collaboration and independent working capabilities
Why Join Thermo Fisher Scientific?
Thermo Fisher Scientific offers professionals an opportunity to:
- Work on global clinical trials across multiple therapeutic areas
- Gain experience in advanced trial data analytics and centralized monitoring
- Collaborate with international pharmaceutical and biotechnology companies
- Develop expertise in clinical research operations and risk-based monitoring
- Build a long-term career with one of the world’s leading scientific organizations
- Work in an innovative, collaborative, and growth-oriented environment
How to Apply
