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Analyst, Analytical Monitor - Bangalore / Hyderabad / Mumbai

Johnson & Johnson
Johnson & Johnson
2+ years
Not Disclosed
Bangalore, Hyderabad, Mumbai, India
10 March 26, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Johnson & Johnson – Analyst, Analytical Monitor | Bangalore / Hyderabad / Mumbai | Hybrid

Company: Johnson & Johnson
Location: Bangalore / Hyderabad / Mumbai, India
Job Type: Full-Time
Work Mode: Hybrid Work Model
Experience: Entry-Level / Early Career (Clinical Data / Analytics)
Qualification: Bachelor’s Degree (Health Sciences, Life Sciences, Data Sciences, or related field)
Compensation: Not disclosed in the job description

Healthcare data analytics and clinical data management jobs in India are growing rapidly, and this role offers an opportunity to work on global clinical trials, risk-based monitoring, and advanced data analytics within the pharmaceutical and biotech industry.

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Job Summary

Johnson & Johnson is hiring an Analyst, Analytical Monitor to support clinical trial monitoring using advanced data analytics, central monitoring, and risk-based monitoring strategies. This role focuses on identifying trends, signals, and potential risks in clinical trial data to improve site performance, ensure patient safety, and maintain data integrity.

You will work closely with Site Managers, Central Monitoring teams, and Clinical Operations experts to enable smarter clinical trial oversight using technology-driven monitoring approaches. This role is ideal for candidates interested in clinical research, clinical data management, central monitoring, and pharmaceutical data analytics careers.


Key Responsibilities

Clinical Trial Data Monitoring

  • Perform analytical monitoring activities across multiple clinical trials.

  • Review site-level and subject-level data to detect trends, anomalies, and risks early.

  • Support execution and close-out of analytical monitoring processes.

Risk-Based Monitoring & Data Quality

  • Identify potential risks related to site performance, participant safety, and data integrity.

  • Support Risk-Based Monitoring (RBM) and Risk-Based Quality Management (RBQM) strategies.

  • Ensure compliance with clinical research regulations and internal SOPs.

Data Analytics & Insights

  • Use reporting tools, analytics platforms, and databases to analyze clinical trial data.

  • Provide actionable insights to Site Managers for site prioritization and decision-making.

  • Support early signal detection and issue prevention in clinical trial operations.

Cross-Functional Collaboration

  • Collaborate with Clinical Operations, Data Management, Central Monitoring, and Clinical Programmers.

  • Communicate effectively across stakeholders and manage multiple communication streams.

  • Follow escalation pathways for identified risks or operational challenges.

Process Improvement & Innovation

  • Participate in analytical tool improvements and process innovation initiatives.

  • Support user acceptance testing (UAT) and requirements development for monitoring tools.

  • Identify opportunities to enhance clinical trial monitoring efficiency.


Required Skills & Qualifications

  • Bachelor’s degree in Life Sciences, Health Sciences, Pharmacy, Biotechnology, or Data Science

  • Experience in data analysis, reporting tools, and analytics platforms

  • Understanding of clinical trial processes and pharmaceutical industry operations

  • Knowledge of:

    • Good Clinical Practice (ICH-GCP)

    • Clinical Data Management

    • Standard Operating Procedures (SOPs)

  • Strong analytical thinking and problem-solving skills

  • Ability to work with cross-functional global teams

  • Excellent written and verbal communication in English

Preferred Skills (Highly Valuable for Candidates):

  • Central Monitoring in clinical trials

  • Risk-Based Monitoring (RBM)

  • Risk-Based Quality Management (RBQM)

  • Quality by Design (QbD)

  • Biostatistics and statistical analysis

  • Clinical operations and project coordination

  • Database applications and data privacy standards

  • Advanced analytics and report writing


Perks & Benefits

  • Opportunity to work with one of the world’s leading pharmaceutical and healthcare companies

  • Exposure to global clinical trials and advanced monitoring technologies

  • Hybrid work environment

  • Inclusive and diverse workplace culture

  • Career growth in clinical research, data analytics, and drug development

  • Collaboration with global healthcare innovation teams


About the Company

Johnson & Johnson is a global leader in pharmaceuticals, biotechnology, and medical technology innovation. The company focuses on advancing healthcare through cutting-edge drug development, clinical research, and digital health solutions that improve patient outcomes worldwide.


Why This Job is Important in Pharma Careers

Roles like Analytical Monitor and Clinical Data Analyst are becoming critical in modern clinical trials. Pharmaceutical companies are shifting toward data-driven monitoring, centralized risk detection, and advanced analytics to ensure faster drug development and improved patient safety.

This position is an excellent entry point for professionals looking to build careers in:

  • Clinical Data Management

  • Clinical Research

  • Pharmacovigilance and Drug Safety Analytics

  • Biostatistics and Data Science in Pharma


Application Process

Interested candidates who want to build a career in clinical research, pharmaceutical data analytics, and clinical trial monitoring should apply through the official Johnson & Johnson careers portal.

Tip: Tailor your resume with keywords like Clinical Data Management, RBM, GCP, Clinical Trials, Data Analytics, Biostatistics, and Central Monitoring to improve selection chances.