PHARMAFull-time
Centralized Monitoring Analyst (Level I & II)
By Admin · Clinical Research & Clinical Operations
BANGALORE (IN)HYBRIDPOSTED: 9/21/2026
PHARMAFull-time
HIRING ORGANIZATIONTHERMO FISHER SCIENTIFICLife Sciences / Scientific Instruments / Biotechnology
ROLE OVERVIEW
Centralized Monitoring Analyst role supporting clinical trials through analysis of operational and patient data, identification of trends and risks, documentation of findings and centralized monitoring activities.
ROLE DEFINITION & RESPONSIBILITIES
- •Review clinical trial data using centralized monitoring tools and systems
- •characterize and track issues, signals and potential risks
- •document monitoring results according to department procedures
- •support development of risk characterization and reporting
- •support review setup and maintain department databases
- •pull and review study reports
- •extract relevant information from protocols and electronic study-data systems
- •identify trends in site and study data
- •prioritize and manage workload according to project demands
- •maintain confidentiality of clinical and client proprietary data
- •communicate findings and potential risks to project teams
Reporting Hierarchy: Works with direct supervision and supports senior team members; collaborates with project teams and internal customers involved in clinical-trial operations and centralized monitoring
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Bachelor's degree or equivalent relevant academic/vocational qualification
- 2+ years of relevant experience
- ability to work under regulatory guidelines, global SOPs and client expectations
- strong analytical and problem-solving ability
- good English communication skills
- understanding of clinical trial processes and documentation
PREFERRED QUALIFICATIONS
- •Previous experience in clinical monitoring, data management, biostatistics or a related clinical-trial field
- •experience with centralized monitoring plans
- •knowledge of medical or therapeutic areas and medical terminology
- •experience using interactive clinical data systems
REQUIRED VERIFIED SKILLS
centralized monitoring
clinical trial data analysis
risk identification
trend analysis
clinical research
data interpretation
regulatory compliance
SOP adherence
analytical problem solving
clinical trial documentation
MS Office
CTMS/data systems
medical terminology
workload management
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Professional development and collaborative global work environment; benefits applicable to the role
No salary or bonus/equity information is disclosed in the supplied posting.
ORGANIZATION CONTEXT & CULTURE
Thermo Fisher Scientific is a global scientific and healthcare company providing products, services and solutions supporting research, clinical development, diagnostics and laboratory operations.
TEAM SIZE: Large multinational organization
INDUSTRY: Life Sciences / Scientific Instruments / Biotechnology
Culture: Collaborative, innovation-focused and scientifically driven environment emphasizing operational excellence, development and scientific excellence.
EXPECTED CAREER ROADMAP
Potential progression within clinical operations and clinical data analytics toward senior centralized monitoring, clinical data management, trial analytics or clinical operations roles, subject to performance and organizational opportunities.
APPLICATION ADVISORY
Emphasize 2+ years of relevant clinical-trial experience, analytical and problem-solving skills, clinical monitoring/data-management knowledge, centralized monitoring exposure, regulatory/SOP compliance and strong Excel/data-system capabilities.
RECOMMENDED TRAINING
1/5
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