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Senior Cdc

ICON
3-5 years
₹8–13 LPA
Bangalore, Remote, India, India
15 July 7, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

Senior CDC (Senior Clinical Data Coordinator)

Company: ICON plc
Location: Bangalore, India
Work Mode: Office or Home (Hybrid/Remote)
Department: Clinical Data Management
Employment Type: Full-Time

Experience: 3–5 years of experience in Clinical Data Management with expertise in eCRF management, clinical data review, data reconciliation, and query management.
Salary Package: ₹8–13 LPA (Approx., based on current market standards; final compensation depends on candidate experience, technical expertise, and clinical data management exposure.)


Role Overview

The Senior Clinical Data Coordinator (Senior CDC) is responsible for supporting clinical data management activities by ensuring accurate, complete, and high-quality clinical trial data. The role collaborates with Clinical Data Management Study Leads and cross-functional teams to manage eCRFs, perform data reconciliation, resolve data issues, and ensure compliance with regulatory standards.


Key Responsibilities

Clinical Data Management

  • Support the Clinical Data Management Study Lead in managing clinical trial data.

  • Assist in the maintenance of:

    • Electronic Case Report Forms (eCRFs)

    • Data Validation Specifications (DVS)

    • Study-Specific Procedures (SSPs)

  • Ensure data quality, completeness, and consistency throughout the study lifecycle.


Data Review & Reconciliation

  • Perform clinical and third-party data reconciliation based on approved edit specifications and data review plans.

  • Review clinical trial data for accuracy, completeness, and protocol compliance.

  • Identify, investigate, and resolve data discrepancies.

  • Ensure timely completion of data cleaning activities.


Data Quality & Issue Management

  • Address data-related queries from project teams and stakeholders.

  • Identify root causes of data issues and recommend effective corrective actions.

  • Monitor and improve overall data quality and integrity.

  • Support database quality control and validation activities.


Project Tracking & Reporting

  • Track study progress and data management task metrics.

  • Communicate project status and performance metrics to:

    • Clinical Data Scientists

    • Study Teams

    • Functional Management

  • Support timely delivery of clinical data management milestones.


Cross-Functional Collaboration

  • Collaborate with Clinical Data Scientists, Biostatistics, Clinical Operations, Medical Writing, and other project stakeholders.

  • Participate in project meetings and contribute to data management discussions.

  • Support continuous process improvement initiatives.

  • Ensure adherence to project timelines and quality standards.


Educational Qualification

  • Bachelor's degree in:

    • Life Sciences

    • Pharmacy

    • Biotechnology

    • Healthcare

    • Or another relevant discipline


Required Experience

  • 3–5 years of experience in Clinical Data Management within the pharmaceutical, biotechnology, or CRO industry.

  • Experience managing eCRFs, data review, and reconciliation activities.

  • Knowledge of clinical trial processes and clinical data standards.

  • Experience working with cross-functional clinical project teams.


Technical Skills

  • Hands-on experience with Clinical Data Management systems such as:

    • Medidata Rave

    • Oracle RDC

    • Other Electronic Data Capture (EDC) platforms

  • Knowledge of:

    • eCRF design and maintenance

    • Data Validation Specifications (DVS)

    • Clinical data reconciliation

    • Query management

  • Good understanding of ICH-GCP guidelines and clinical data management best practices.

  • Proficiency in Microsoft Office Suite.


Key Competencies

  • Strong analytical and problem-solving skills.

  • Excellent attention to detail and data accuracy.

  • Strong organizational and time management abilities.

  • Effective communication and interpersonal skills.

  • Ability to work independently and collaboratively in a cross-functional environment.

  • Strong stakeholder management and coordination skills.

  • Commitment to quality, compliance, and continuous improvement.

  • Ability to manage multiple clinical studies and meet project deadlines.