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Centralized Monitoring Analyst (Level I & Ii)

Thermo Fisher Scientific
2+ years
₹6–10 LPA
Bangalore, Hyderabad, Remote, India, India
15 July 16, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding

Job Title: CM Analyst I (Trial Data Analytics Specialist II)

Company: Thermo Fisher Scientific

Location: India

Employment Type: Full-time

Work Schedule: Second Shift (Afternoons)

Work Environment: Office

Experience Required: 2+ years of experience in Clinical Monitoring, Clinical Data Management, Biostatistics, or Clinical Trial Analytics.

Education: Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Nursing, Statistics, or a related field.

Salary Package: ₹6–10 LPA (Estimated as per current market standards; final compensation depends on experience, skills, and location.)

Key Responsibilities:

  • Review clinical trial data using centralized monitoring tools and systems.

  • Identify, characterize, and track clinical data issues, trends, and potential risks.

  • Document review findings in accordance with departmental procedures.

  • Support risk characterization and reporting activities.

  • Assist in centralized monitoring setup, including report generation and database updates.

  • Analyze operational and patient clinical trial data.

  • Communicate findings and potential risks to project teams.

  • Ensure compliance with regulatory guidelines, SOPs, and study protocols.

  • Support ongoing clinical trial monitoring and data quality activities.

Required Skills:

  • Centralized Monitoring (CM)

  • Clinical Trial Data Review

  • Clinical Data Analytics

  • Risk Identification & Assessment

  • Clinical Data Management (CDM)

  • Clinical Monitoring

  • Data Analysis & Interpretation

  • Microsoft Office (Excel, Word, PowerPoint)

  • Analytical & Problem-Solving Skills

  • Attention to Detail

  • Medical Terminology

  • Regulatory Compliance (GCP/SOPs)

  • Communication & Documentation

  • Time Management

Preferred Skills:

  • Experience in Clinical Monitoring or Clinical Data Management.

  • Knowledge of Biostatistics and Clinical Trial Operations.

  • Familiarity with Centralized Monitoring Plans and Electronic Clinical Data Systems.

  • Understanding of clinical protocols and therapeutic areas.

Work Mode: Office-Based

Benefits:

  • Competitive salary and career growth opportunities.

  • Work on global clinical trials with leading pharmaceutical and biotech companies.

  • Exposure to advanced clinical data analytics and centralized monitoring.

  • Learning and development opportunities.

  • Collaborative and innovation-driven work environment.

  • Global career opportunities within Thermo Fisher Scientific.