Instagram
youtube
Facebook

Senior Cdc

6+ years
Not Disclosed
10 Dec. 2, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Senior Clinical Data Coordinator (Senior CDC) – India
Company: ICON plc
Job ID: JR139465
Work Mode: Office with Flex
Locations: Bangalore / Trivandrum / Chennai
Job Type: Full-time
Application Deadline: December 4, 2025


About ICON plc

ICON plc is a global leader in healthcare intelligence and clinical research services. The organization is committed to innovation, scientific excellence, and inclusive growth. As part of ICON, you will contribute to shaping the future of clinical development through high-quality data management and operational excellence.


Role Overview

The Senior Clinical Data Coordinator (Senior CDC) will support data management operations for global clinical trials. This role requires expertise in eCRF maintenance, data review planning, and cross-functional communication to ensure accurate, compliant, and high-quality clinical data delivery.


Key Responsibilities

Clinical Data Management

  • Support the Data Management Study Lead in maintaining eCRF, Data Validation Specifications, and Study-Specific Procedures.

  • Manage clinical and third-party data reconciliation according to edit checks and data review plans.

  • Track study metrics, task progress, and data quality indicators while ensuring timely communication with project teams and functional stakeholders.

Data Quality & Issue Resolution

  • Respond to data-related queries and recommend feasible solutions.

  • Identify root causes of data discrepancies and contribute to systematic corrections.

  • Ensure adherence to internal SOPs, regulatory expectations, and project timelines.

Cross-functional Collaboration

  • Work closely with clinical data scientists, project managers, and other cross-functional teams to support study progress.

  • Contribute to process improvements and documentation updates as required.


Required Qualifications & Experience

  • Education: Bachelor’s degree in Life Sciences, Healthcare, or a related field.

  • Experience: Minimum 6 years of clinical data management experience within the pharmaceutical, CRO, or biotechnology industry.

  • Technical Skills:

    • Proficiency with clinical data management systems such as Medidata Rave, Oracle RDC, or similar platforms.

    • Strong understanding of clinical data workflows and edit check specifications.

  • Additional Skills:

    • Strong attention to detail, ability to work in fast-paced environments.

    • Excellent communication and teamwork capabilities.

    • Familiarity with ICH-GCP or regulatory guidelines is preferred.


Benefits Offered by ICON

ICON provides competitive compensation and a comprehensive benefits package designed for employee well-being and work–life balance. Benefits vary by country and may include:

  • Annual leave entitlements

  • Health insurance plans for employees and dependents

  • Retirement planning and financial benefits

  • Global Employee Assistance Programme (TELUS Health)

  • Life assurance

  • Additional country-specific voluntary benefits such as childcare vouchers, travel passes, gym discounts, and more

More information is available on the ICON careers website.


Commitment to Inclusion & Equal Opportunity

ICON is dedicated to creating an inclusive, accessible, and discrimination-free workplace. All qualified candidates are encouraged to apply, including individuals requiring accommodations due to medical conditions or disabilities.

Candidates who may not meet every requirement are still encouraged to apply, as ICON values diverse strengths and potential.


Internal Applicants

Current ICON employees should apply via the Internal Employee Portal.