Thermo Fisher Scientific is inviting applications for the position of Centralized Monitoring Analyst (Level I & II) in Bangalore and Hyderabad, India. This full-time opportunity is listed under a hybrid work arrangement, with the work schedule specified as the second shift (afternoons).
The role focuses on reviewing clinical trial and operational data to identify trends, potential risks, and data-related issues. Selected candidates will support centralized monitoring activities, document findings, track risk signals, and communicate observations to clinical project teams for appropriate follow-up.
This opportunity may suit graduates with experience in clinical monitoring, clinical data management, biostatistics, or related areas supporting clinical trials. The supplied job description indicates that comparable experience of approximately two years is expected.
Thermo Fisher Scientific Recruitment 2026: Job Highlights
| Particulars | Details |
|---|---|
| Company | Thermo Fisher Scientific |
| Job Title | Centralized Monitoring Analyst (Level I & II) |
| Job Requisition ID | R-01357990 |
| Job Locations | Bangalore and Hyderabad, India |
| Job Category | Clinical Research / Centralized Monitoring |
| Employment Type | Full-time |
| Work Arrangement | Hybrid listing; office environment specified |
| Work Schedule | Second shift (afternoons) |
| Qualification | Bachelor’s degree or equivalent relevant qualification |
| Experience | Comparable to 2+ years |
| Preferred Background | Clinical monitoring, data management, biostatistics, or related clinical trial experience |
| Salary | Not disclosed |
| Application Mode | Online |
About Thermo Fisher Scientific
Thermo Fisher Scientific is a global science and healthcare company supporting scientific research, clinical development, diagnostics, and laboratory operations. Its work includes services and technologies that help pharmaceutical and biotechnology organizations advance research and drug development.
The centralized monitoring team supports clinical research by reviewing study data, identifying potential risks, and helping project teams maintain data quality and operational oversight.
Job Description: Centralized Monitoring Analyst
The Centralized Monitoring Analyst reviews clinical trial and operational data using designated systems and analytical tools. The role involves identifying patterns, documenting issues, tracking risk signals, and supporting centralized monitoring plans under the guidance of senior team members.
The analyst also helps prepare reports, update departmental databases, and extract relevant information from study documentation. Findings are communicated to project teams so that potential concerns can be evaluated and addressed.
Key Responsibilities
1. Clinical Trial Data Review
- Review clinical trial data using approved tools and systems.
- Perform monitoring activities in accordance with the centralized monitoring plan.
- Identify unusual trends, potential issues, and risk indicators in operational or patient-related study data.
- Extract relevant information from protocols and electronic study data systems.
- Support the identification of trends across study sites and clinical trials.
2. Risk Identification and Tracking
- Characterize and track evidence relating to identified issues, signals, and potential risks.
- Support the assessment of risk patterns in clinical trial operations.
- Communicate findings and potential concerns to project team members.
- Contribute to risk characterization and reporting activities when required.
3. Documentation and Reporting
- Document review findings according to departmental procedures.
- Maintain accurate records of monitoring activities and identified issues.
- Support report generation and data extraction.
- Update departmental databases and assist with setting up monitoring reviews.
4. Project Team Collaboration
- Work with senior team members and clinical project teams.
- Communicate findings clearly to internal stakeholders.
- Support follow-up actions related to identified data quality or operational concerns.
- Manage assigned work according to project priorities and changing deadlines.
Eligibility Criteria
Educational Qualification
Candidates should have a bachelor’s degree or an equivalent relevant academic or vocational qualification.
The company may consider a suitable combination of education, training, and directly related experience where it meets the requirements of the role.
Experience Required
The job description indicates experience comparable to two or more years. Previous experience in any of the following areas is preferred:
- Clinical monitoring.
- Clinical data management.
- Biostatistics.
- Other functions supporting clinical trials.
The posting does not clearly separate the minimum requirements for Level I and Level II. Candidates should review the official application page for any level-specific eligibility criteria.
Required Skills
Applicants should demonstrate the following abilities:
- Strong analytical and problem-solving skills.
- Attention to detail and confidence working with numerical data.
- Knowledge of clinical trial operations and study documentation.
- Understanding of clinical monitoring plans and project protocols.
- Familiarity with medical terminology and therapeutic areas.
- Ability to recognize data trends and potential risks.
- Good written and spoken English.
- Working knowledge of Microsoft Word, Excel, and PowerPoint.
- Ability to manage multiple tasks and changing priorities.
- Strong organizational and time-management skills.
- Ability to work independently and collaboratively.
- Understanding of confidentiality requirements for clinical and client data.
- Willingness to follow regulatory guidelines, global SOPs, and client requirements.
Work Location and Shift Details
The job is listed for the following locations:
- Bangalore, Karnataka, India
- Hyderabad, Telangana, India
The listing indicates a hybrid work arrangement, while the environmental conditions specify an office setting. Candidates should confirm the applicable office attendance requirements during the recruitment process.
Shift: Second shift, during afternoon hours. The exact working hours are not specified in the supplied description.
The role may involve working in office, laboratory, or clinical environments, depending on operational requirements. The posting also mentions potential exposure to biological fluids and infectious organisms in relevant work settings, with personal protective equipment required where applicable.
Salary and Benefits
Thermo Fisher Scientific has not disclosed a specific salary range for this position in the supplied job description.
The company highlights a collaborative work environment, opportunities for professional development, and the chance to contribute to scientific and clinical research. Candidates should confirm the applicable compensation, benefits, shift allowance, and work arrangement through the official recruitment process.
How to Apply for Thermo Fisher Scientific Recruitment 2026
Interested and eligible candidates can apply through the company’s official careers portal.
Before applying, prepare an updated resume highlighting your clinical trial experience, data review and analysis skills, knowledge of study documentation, and proficiency in Microsoft Excel.
Review the official listing carefully to confirm the requirements for the applicable level and preferred work location.
Frequently Asked Questions (FAQs)
1. Which company is hiring for Centralized Monitoring Analyst jobs?
Thermo Fisher Scientific is recruiting for the Centralized Monitoring Analyst (Level I & II) position.
2. Where are these jobs located?
The listed locations are Bangalore and Hyderabad, India.
3. What is the job requisition ID?
The requisition ID is R-01357990.
4. What qualification is required?
A bachelor’s degree or equivalent relevant academic or vocational qualification is specified.
5. How much experience is required?
The description indicates experience comparable to two or more years. Clinical monitoring, clinical data management, biostatistics, or related clinical trial experience is preferred.
6. Is this a work-from-home job?
The listing shows a hybrid arrangement, but the environmental conditions specify an office setting. Candidates should confirm the applicable arrangement with the employer.
7. What shift will the selected candidate work?
The advertised schedule is the second shift, during afternoon hours. Exact timings are not provided.
8. What are the main responsibilities?
The role includes reviewing clinical trial data, identifying trends and potential risks, documenting findings, supporting centralized monitoring reports, and communicating issues to project teams.
9. What is the salary for this position?
The salary is not disclosed in the supplied job details.
10. How can candidates apply?
Candidates can submit their application through the official Thermo Fisher Scientific careers link included above.
Disclaimer
This article is a rewritten summary of the supplied Thermo Fisher Scientific job listing. Vacancy status, eligibility requirements, shift timings, compensation, and work arrangements may change. Candidates should verify the latest information on the official application page before applying.