Centralized Monitoring Analyst

Thermo Fisher Scientific India Pvt Ltd; Bengaluru; On-site; INR 550,000 - 850,000; Full time

Job summary

Thermo Fisher Scientific India Pvt Ltd in Bengaluru is seeking a Centralized Monitoring Analyst I–II for afternoon shifts. You will review clinical trial data, identify risks, and support the centralized monitoring plan under senior team guidance.

The role emphasizes data review, risk characterization, documentation, and collaboration with project teams to ensure compliance with SOPs and regulatory requirements; a Bachelor's degree and 2+ years' experience are preferred.

Qualifications

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification.
• 2+ years’ experience in clinical monitoring, data management, biostatistics or related field in support of clinical trials preferred.

Responsibilities

• Reviews clinical trial data using tools and systems in alignment with the centralized monitoring plan with support from senior team members.
• Characterizes and tracks evidence of issues, signals and potential risks with support from senior team members.
• Ensures results of reviews are documented per department procedures.
• May participate in development of risk characterization and reporting.
• Supports review setup, including updating department database, pulling reports, etc.

Skills

Analytical skills

Attention to detail

Problem solving

Communication skills

MS Office

Teamwork

Confidentiality

Time management

Prioritization

Regulatory knowledge

Education

Bachelor's degree

Tools

MS Office

Job description

Centralized Monitoring Analyst (Level I & II) Work Schedule Second Shift (Afternoons) Environmental Conditions Office Job Description

Join Us as a CM Analyst I– Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in organizational performance. As a Trial Data Analytics Specialist II, you will identify and characterize issues and trends in operational and patient clinical trial data using analytical or statistical tools. You will leverage your operational experience and knowledge to evaluate issues and develop findings based on the data analyzed, communicating issues and potential risks to project team members for follow-up action.

What You’ll Do:

• Reviews clinical trial data using a variety of tools and systems in alignment with the centralized monitoring plan with support from senior team members.
• Characterizes and tracks the evidence of issues, signals and potential risks with support from senior team members.
• Ensures results of reviews are appropriately documented per department procedures.
• May participate in development of risk characterization and reporting.
• Supports review set-up, including updating department database, pulling reports, etc.

Education and Experience Requirements:

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years’). Prior experience in clinical monitoring, data management, biostatistics or related field in support of clinical trials is preferred. In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

• Capable of applying fundamental knowledge and skills in a highly organized fashion while adhering to
• regulatory guidelines, global SOPs and client expectations
• Strong attention to detail and skill with numbers
• Good analytical /problem-solving skills /judgment in decision making
• Ability to work productively with direct supervision
• Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data
• Flexibility and adaptability
• Ability to work in a team environment and independently
• Good oral and written communication skills (English) with the ability to communicate with a variety of
• internal customers, including project team
• Good computer skills, with knowledge of MS Office (Word, Excel, PowerPoint) and the ability to learn
• and use interactive computer systems
• Ability to extract pertinent information from standard study documentation, such as protocols,
• electronic study data systems with the ability to learn to identify trending of site/study data
• Prioritization skills with ability to plan, monitor and manage workload fluidly in response to changing
• project demands
• Satisfactory understanding of project protocol, project documentation including Centralized
• Monitoring Plan and other functional plans
• Broad working knowledge of the roles, functions and process of conducting clinical trials
• Broad understanding of medical/therapeutic area knowledge and of medical terminology

Working Conditions and Environment:

• Work is performed in an office/ laboratory and/or a clinical environment.
• Exposure to biological fluids with potential exposure to infectious organisms.
• Exposure to electrical office equipment.
• Personal protective equipment required such as protective eyewear, garments and gloves

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.