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Analyst Central Monitoring Expert - Hyderabad/Bangalore/Mumbai

Johnson & Johnson
Johnson & Johnson
0-3 years
Not Disclosed
Bangalore, Hyderabad, Mumbai, India
10 April 24, 2026
Job Description
Job Type: Full Time Hybrid Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Analyst Central Monitoring Expert (Clinical Data Analytics & RBQM) – Hyderabad / Bangalore / Mumbai | Johnson & Johnson Careers

About Johnson & Johnson
Johnson & Johnson is a global leader in healthcare innovation, committed to transforming patient outcomes through advancements in pharmaceuticals, biotechnology, and medical technology. Guided by its long-standing Credo, the organization fosters an inclusive, diverse, and purpose-driven workplace while delivering breakthrough solutions that improve health worldwide.

Job Overview
Johnson & Johnson is hiring an Analyst Central Monitoring Expert to support central monitoring and Analytical Risk-Based Monitoring (ARBM) activities for clinical trials. This entry-level role focuses on leveraging data analytics to enhance patient safety, ensure data quality, and optimize clinical trial oversight through risk-based monitoring strategies.

Job Location & Work Model

  • Locations: Hyderabad, Bangalore, Mumbai (India)

  • Work Type: Hybrid

  • Job Category: Clinical Data Management / Data Analytics

Key Responsibilities

Core Central Monitoring Activities

  • Support execution of central monitoring and ARBM activities across multiple clinical trials

  • Ensure compliance with SOPs, regulatory guidelines, and internal policies

  • Analyze clinical trial data using dashboards, reporting tools, and analytics platforms

  • Identify potential risks, trends, and data quality issues at site and subject levels

  • Document risks and support resolution tracking and reporting

Central Monitoring Manager Responsibilities (as applicable)

  • Contribute to development and improvement of ARBM models and processes

  • Support study start-up activities including protocol risk assessment and de-risking strategies

  • Assist in developing integrated risk management plans and monitoring guidelines

  • Participate in Central Monitoring Working Group (CMWG) discussions

  • Identify Critical-to-Quality (CtQ) factors and contribute to study-specific reports

  • Provide guidance and training to Analytical Monitors where required

Analytical Monitoring Responsibilities (as applicable)

  • Conduct periodic analytical reviews to detect early signals and prevent issues

  • Collaborate with Site Managers and study teams to address trends and risks

  • Utilize clinical systems and databases to monitor compliance, safety, and data integrity

  • Provide actionable insights to support site prioritization and engagement decisions

Cross-Functional Collaboration

  • Work closely with Data Management teams, Clinical Operations, Biostatistics, and Trial Management teams

  • Communicate effectively across multiple stakeholders and escalate issues when necessary

  • Support process improvement initiatives and innovation projects, including tool development and user acceptance testing

Required Skills and Competencies

  • Strong analytical and data interpretation skills

  • Understanding of clinical data management and clinical trial processes

  • Knowledge of Good Clinical Practice (GCP) and regulatory standards

  • Ability to work with data systems, dashboards, and reporting tools

  • Strong communication and stakeholder management skills

  • Ability to manage multiple tasks and collaborate in cross-functional environments

  • High attention to detail and quality

Technical Skills

  • Experience with data analytics tools and clinical data platforms

  • Familiarity with database applications and reporting systems

  • Knowledge of RBQM (Risk-Based Quality Management), RBM (Risk-Based Monitoring), and QbD (Quality by Design) concepts (preferred)

  • Basic understanding of biostatistics and risk management principles (preferred)

Educational Qualifications

  • Bachelor’s degree in Health Sciences, Life Sciences, Data Sciences, or related field

  • Equivalent professional experience may be considered

Experience Requirements

  • Minimum: 0–2 years of experience in data analytics, clinical data management, or related field

  • Freshers: Eligible (with relevant academic background or internship experience)

  • Preferred: Exposure to clinical research, pharmaceutical industry, or data-driven environments

Why Join Johnson & Johnson

  • Work with a global leader in healthcare innovation

  • Gain hands-on experience in advanced clinical data analytics and risk-based monitoring

  • Collaborate with cross-functional global teams

  • Opportunity to contribute to improving patient safety and clinical trial quality

  • Inclusive, diverse, and growth-oriented work environment

Diversity, Equity, and Inclusion
Johnson & Johnson is committed to creating an inclusive workplace where diversity is valued, and every employee is empowered to contribute and grow.

Application Process
All applications are reviewed through Johnson & Johnson’s official recruitment process. Candidates are encouraged to apply through the company’s careers portal for timely updates.

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