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Analytical Monitor

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ICON
4+ years
₹12 LPA – ₹20 LPA (Estimated)
Bangalore, Chennai, Trivandrum, India
10 March 11, 2026
Job Description
Job Type: Full Time 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

Job Title: Analytical Monitor

Location: Bangalore, Chennai, Trivandrum, India (Office With Flexibility)

Company: ICON plc

Employment Type: Full-time

Salary: ₹12 LPA – ₹20 LPA (Estimated)


Job Description

ICON plc is seeking an Analytical Monitor to join its Integrated Data Analytics & Reporting team. In this role, you will help identify site-level and subject-level risks in clinical trials using advanced data analytics, supporting improved trial quality, patient safety, and operational efficiency.

You will work across multiple clinical studies, analyzing data trends and collaborating with cross-functional teams to ensure data-driven risk management and proactive monitoring throughout the clinical trial lifecycle.


Key Responsibilities

  • Perform analytical monitoring activities across assigned clinical trials to identify early data risks and trends.

  • Conduct site-level and subject-level data reviews to detect potential issues and ensure data quality.

  • Analyze data from multiple platforms, reporting systems, and databases to generate actionable insights.

  • Collaborate with Site Managers, Central Monitoring teams, and other stakeholders to support risk-based monitoring strategies.

  • Ensure compliance with SOPs, ICH-GCP guidelines, and regulatory requirements.

  • Communicate findings effectively and escalate issues through established processes.

  • Provide training, mentorship, and guidance to junior analytical monitors.


Required Qualifications

  • Bachelor’s degree in Health Sciences, Data Science, or a related field (Master’s degree preferred).

  • 4+ years of experience in the pharmaceutical, biotechnology, or CRO industry.

  • Strong understanding of clinical trial operations and clinical data workflows.

  • Experience performing data analysis within a clinical research environment.


Preferred Skills

  • Knowledge of risk-based monitoring and clinical data analytics methodologies.

  • Familiarity with clinical data platforms and reporting tools.

  • Strong understanding of statistical concepts and clinical trial data interpretation.

  • Experience in project, issue, and risk management.

  • Excellent communication and collaboration skills for working with global teams.

  • Strong organizational abilities and capability to manage multiple projects simultaneously.


Benefits

Employees at ICON plc may receive benefits such as:

  • Competitive salary and performance incentives

  • Paid annual leave and holidays

  • Comprehensive health insurance plans for employees and families

  • Retirement savings and financial planning programs

  • Global Employee Assistance Programme (TELUS Health) for wellbeing and mental health support

  • Life insurance coverage

  • Flexible benefits such as childcare support, gym memberships, travel subsidies, and wellness programs


About the Company

ICON plc is a leading healthcare intelligence and clinical research organization partnering with pharmaceutical, biotechnology, and medical device companies to accelerate clinical development and bring innovative therapies to patients worldwide.