Johnson & Johnson Hiring Fresher for Analyst- Analytical Monitor Role

ByPharma Hiring Hub

Johnson & Johnson, a global leader in healthcare and pharmaceuticals, is hiring for the role of Analyst, Analytical Monitor across Bangalore, Hyderabad, and Mumbai. This is a strong entry‑level opportunity for professionals interested in clinical data management, central monitoring, and Risk‑Based Monitoring (RBM) within a regulated pharmaceutical environment.

The role focuses on supporting data‑driven clinical trial monitoring, RBQM analytics, and centralized oversight activities to help ensure data quality, patient safety, and operational efficiency. Candidates will collaborate with cross‑functional clinical teams and contribute to global clinical trial operations using advanced analytics and monitoring tools.

This position is ideal for individuals aiming to build a career in clinical research analytics, centralized monitoring, and modern risk‑based clinical trial oversight.

Johnson & Johnson Career

Job Overview

  • Position: Analyst, Analytical Monitor
  • Department: CDM
  • Location: Hyderabad, Bangalore, Mumbai
  • Experience: 0 to 2 Years
  • Qualification: B.Pharm, M.Pharm, Pharma.D, B.Sc, M.Sc
  • Job Type: Full-Time
  • Last Date of application: 1 April 2026

Key Responsibilities – Analyst, Analytical Monitor

  • SOP & Process Compliance: Perform assigned activities in full compliance with Johnson & Johnson functional SOPs, processes, and policies.
  • Communication & Escalation
    • Facilitate clear and effective communication while managing multiple communication streams.
    • Follow established escalation pathways to address issues in a timely manner.
  • Process Improvement & Innovation Support: Contribute to process improvement and innovation initiatives, including participation in requirements gathering, User Acceptance Testing (UAT), and identification of enhancements for analytical tools and systems.
  • Central & Analytical Monitoring: Perform analytical monitoring activities for assigned clinical trials in alignment with portfolio timelines, priorities, execution, and study close‑out processes.
  • Site & Subject‑Level Risk Review: Conduct regular, fit‑for‑purpose site‑ and subject‑level reviews to enable early detection of risks and prevent recurrence of issues.
  • Trend & Signal Management: Collaborate closely with Site Managers and Central Monitoring Managers to evaluate trends and signals, and support appropriate actions at site and subject levels.
  • Risk Identification & Data Review: Access and analyze data from multiple systems, databases, and reporting tools to identify risks related to:
    • Data quality
    • Study participant safety
    • Protocol compliance
  • Analytical Insights & Decision Support: Provide timely analytical insights to support Site Managers in site prioritization, targeted engagement, and risk‑based decision‑making.
  • Internal Stakeholders: Collaborate with J&J Innovative Medicine teams including Site Managers and Local Trial Managers.
  • Work closely with IDAR functions such as Central Monitoring, Data Management, Data Acquisition Experts, Clinical Programmers, and Functional Leadership.
  • External Stakeholders: Coordinate with external suppliers and service partners supporting analytical monitoring and clinical trial operations.

Required Skills & Qualifications

  • Educational Background: Bachelor’s degree (BS, BA) or equivalent professional experience, preferably in Health Sciences, Data Sciences, or a related discipline.
  • Data & Technical Experience
  • Experience with data analysis, including interpretation of trends and review of analytical outputs.
  • Experience working with technology platforms and systems used for data collection, analysis, and reporting in a regulated environment.
  • Collaboration & Coordination Skills
  • Ability to collaborate effectively with cross‑functional stakeholders.
  • Strong skills in planning, coordinating, and managing tasks across multiple priorities.
  • Communication Skills: Effective written and verbal communication skills in English, with the ability to clearly present insights and findings.
  • Preferred Qualifications
  • Clinical Research Knowledge: Understanding of clinical drug development within the pharmaceutical or related industry.
  • Risk & Quality Concepts: Familiarity with risk management, project management, and/or basic statistical concepts.
  • RBQM / Central Monitoring Exposure: Knowledge of Central Monitoring, Risk‑Based Quality Management (RBQM), Risk‑Based Monitoring (RBM), and Quality by Design (QbD) principles is an advantage.

Why Join Johnson&Johnson?

  • Global Healthcare Leader
  • Be part of one of the world’s most trusted and established healthcare organizations, supporting innovation across pharmaceuticals, medical devices, and healthcare solutions.
  • Data‑Driven Clinical Research Environment
  • Gain hands‑on exposure to analytical monitoring, central monitoring, and risk‑based quality management (RBQM) within modern, data‑driven clinical trials.
  • Strong Foundation for Early‑Career Growth
  • The Analyst, Analytical Monitor role offers a solid entry point into clinical research analytics, helping you build expertise in RBM, data interpretation, and trial oversight.
  • Cross‑Functional Collaboration
  • Work closely with Site Managers, Clinical Operations, Data Management, Central Monitoring teams, and other stakeholders across global studies.

How to Apply

Interested candidates should apply only through the official company career website using the link provided below.

Apply Here

Important Disclaimer

This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.

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FAQ – Analyst, Analytical Monitor

1. Who can apply for the Analyst, Analytical Monitor role?

Candidates with a Bachelor’s degree in Health Sciences, Data Sciences, or a related field, or equivalent professional experience, are eligible to apply.

2. Is this role suitable for entry‑level candidates?

Yes. This is a strong entry‑level opportunity for professionals interested in clinical research analytics, central monitoring, and RBM/RBQM practices.

3. What are the main responsibilities of this role?

You will perform analytical and central monitoring activities, review site and subject‑level data, identify risks and trends, and support risk‑based decision‑making for clinical trials.

4. Will I work on global clinical trials?

Yes. The role supports global clinical studies, working closely with cross‑functional teams across regions.

5. What systems or tools will I use?

You will use clinical data systems, databases, and reporting tools to monitor trial performance, data quality, and participant safety.

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