Hybrid Clinical Research Job at ICON | Life Science Graduates Must Apply! A job advertisement banner from Biotecnika for a Clinical Research position at ICON. The top center features the "biotecnika" logo with the tagline "Your Bio Resource". Below the logo, a prominent dark grey bar contains the large, bold white text headline: "Hybrid Clinical Research Job at ICON". The main visual is a detailed, realistic illustrative scene of a professional woman in a blazer and headphones seated at a desk with an office cityscape in the background. She is looking at three computer monitors: one showing a "Global Trial Management" data dashboard, another showing a live video conference with a team (labeled "Team Check-in - Remote Site"), and the third is a laptop. Objects on the desk include a coffee mug that reads "COFFEE & CLINICAL DATA", a stack of "Good Clinical Practice Guide" books, and vials. At the bottom center, a pulsing teal-colored rounded rectangular button with white text reads "APPLY NOW".
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Hybrid Clinical Research Job at ICON

Looking for a high-growth Clinical Research Job in India’s booming healthcare and pharmaceutical sector? Here’s an exciting opportunity from ICON plc for passionate candidates seeking a rewarding Life Science Job with hybrid flexibility. ICON Careers is hiring for the role of CDC II in Bangalore, Chennai, and Trivandrum, offering an incredible opportunity for life science graduates to work in clinical data management, clinical trials, and healthcare analytics. If you have experience in clinical data review and dream of building an international research career, this could be your next big breakthrough.

About the Company

ICON plc is a global healthcare intelligence and clinical research organization focused on advancing clinical development through innovation, technology, and data-driven research solutions. The company collaborates with pharmaceutical, biotechnology, and healthcare organizations worldwide.

Job Details:

  • Job Title: CDC II – Clinical Data Management
  • Job ID: JR150695
  • Company: ICON plc
  • Department: Clinical Data Management – ICON Strategic Solutions (FSP)
  • Work Mode: Hybrid
  • Job Locations: Bangalore / Bengaluru, Chennai, Thiruvananthapuram

Role Overview

The CDC II role involves supporting clinical data management activities for clinical trials by reviewing, validating, and analyzing clinical datasets while ensuring data quality, integrity, and regulatory compliance. The position requires close collaboration with Data Management trial partners and cross-functional stakeholders to support efficient clinical trial execution.

The role also contributes to data review strategies, reconciliation activities, audit readiness, and operational decision-making through data visualization and analytics.

Key Responsibilities

  • Clinical Data Review & Validation
    • Review clinical data across databases, datasets, listings, reports, and analytics platforms
    • Ensure data completeness, accuracy, and integrity
    • Raise, review, and close queries in EDC/CDMS systems
    • Support correction and verification of study data by site personnel
  • Data Management Operations
    • Follow Data Management Monitoring (DMM) and Risk Assessment Categorisation Tool (RACT) processes
    • Support development and execution of data review strategies and reports
    • Track and communicate data review status to DM Trial Partners
    • Maintain trial documentation and archival records
  • Collaboration & Trial Support
    • Collaborate with Trial Partners and stakeholders to achieve data review deliverables
    • Support Data Management Study Leads in maintaining:
      • eCRFs
      • Data Validation Specifications
      • Study-Specific Procedures
      • Assist in clinical and third-party data reconciliation activities
  • Risk Management & Issue Resolution
    • Identify and resolve data-related issues
    • Escalate critical findings when necessary
    • Conduct root cause analysis for recurring data issues
    • Support audits and inspections
  • Data Analytics & Visualization
    • Use data visualization techniques to support operational decision-making
    • Effectively communicate data insights and findings
    • Prepare study and task metrics for project teams and management

Educational Qualification: Candidates should possess a Bachelor’s Degree in Life Sciences and Related disciplines.

Required Experience & Skills

  • Intermediate-level experience in Clinical Data Management within the Pharmaceutical and Biotechnology industry
  • Familiarity with Medidata, Oracle RDC, and Similar clinical data management systems
  • Strong attention to detail
  • Ability to work in fast-paced environments
  • Good organizational and analytical skills
  • Excellent communication and collaboration abilities
  • Understanding of ICH-GCP guidelines and Clinical trial data standards

Preferred Competencies

Experience with:

  • Data review workflows
  • Clinical trial reconciliation
  • Query management
  • Risk-based monitoring approaches
  • Ability to independently manage assigned data review activities
  • Strong problem-solving and decision-making skills

Benefits & Perks

Employees may receive access to:

  • Competitive compensation
  • Health insurance benefits
  • Retirement planning support
  • Employee Assistance Programs
  • Life assurance coverage
  • Flexible country-specific benefits
  • Work-life balance initiatives
  • Wellness and family support programs

APPLY ONLINE HERE

Diluxi Arya
Diligence + Intelligence + Learned +Understanding +Xenial + Idealistic = DILUXI. Girl with the golden hands, She has worked hard and transformed BioTecNika's Alerts section with Latest Notifications and Articles with most profound insights. When we need a reliable hand at work, All eyes turn to her!

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