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Data Surveillance Analyst

Parexel
2+ years
INR 6 LPA – 10 LPA
Remote, India, India
1 June 24, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

DATA SURVEILLANCE ANALYST

Company: Parexel
Location: Remote, India
Job ID: R0000042355
Category: Clinical Trials
Job Type: Full-Time

JOB OVERVIEW

The Data Surveillance Analyst (DSA) is responsible for analyzing scientific and operational clinical trial data to support Risk-Based Quality Management (RBQM) and centralized monitoring activities. The role focuses on identifying data quality trends, risk signals, protocol deviations, and operational issues through advanced data surveillance techniques to ensure study quality, patient safety, and regulatory compliance.


KEY RESPONSIBILITIES

• Data Surveillance Plan Development

  • Support the development of Data Surveillance Plans (DSPs).

  • Define and monitor Key Risk Indicators (KRIs).

  • Establish and review Quality Tolerance Limits (QTLs).

  • Support central statistical monitoring activities.

  • Assist in risk assessment and risk mitigation planning.

• Technology Configuration & Management

  • Configure and maintain Data Surveillance platforms such as CluePoints.

  • Create data import mappings from multiple clinical data sources.

  • Configure standard and customized KRIs.

  • Set up statistical analysis parameters.

  • Maintain technology settings throughout the study lifecycle.

• Data Monitoring & Analysis

  • Perform centralized monitoring reviews according to study-specific plans.

  • Analyze scientific and operational study data.

  • Identify trends, outliers, inconsistencies, and potential risks.

  • Detect atypical data patterns and quality signals.

  • Support risk identification and escalation processes.

• Data Quality Surveillance

  • Review Quality Tolerance Limits (QTLs).

  • Monitor protocol compliance and data quality.

  • Evaluate emerging issues affecting study integrity.

  • Support issue resolution and corrective actions.

• Documentation & Reporting

  • Document findings in Data Surveillance Findings Forms.

  • Update issue tracking systems and CluePoints Issue Management.

  • Prepare Central Monitoring Reports.

  • Maintain audit-ready documentation.

  • Track actions and resolutions.

• Stakeholder Collaboration

  • Participate in internal and external Data Surveillance meetings.

  • Present findings to study teams and sponsors.

  • Collaborate with Clinical Operations, Data Management, Biostatistics, and RBQM teams.

  • Support audits and regulatory inspections.

  • Assist project leads in review meetings and decision-making.

• Continuous Improvement

  • Work with technology teams to improve surveillance tools.

  • Recommend process improvements.

  • Support implementation of innovative monitoring strategies.

  • Contribute to RBQM best practices.


REQUIRED QUALIFICATIONS

  • Bachelor's Degree in:

    • Life Sciences

    • Pharmacy

    • Biotechnology

    • Statistics

    • Clinical Research

    • Related Scientific Discipline

Preferred:

  • Master's Degree in Life Sciences, Statistics, Clinical Research, or Data Science


EXPERIENCE

2–5 Years

Preferred experience in:

  • Clinical Data Management

  • Clinical Data Review

  • Risk-Based Monitoring (RBM)

  • Centralized Monitoring

  • Clinical Operations

  • Clinical Research

  • Data Analytics