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Senior Cdc

3-5 years
Not Disclosed
10 May 16, 2025
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: Senior Clinical Data Coordinator (Senior CDC)
Location: Chennai (Office-Based), India
Job ID: 2024-114205
Department: ICON Strategic Solutions – Biometrics Portfolio


Company Overview:

Join ICON plc, the world’s largest and most comprehensive clinical research organization, powered by healthcare intelligence. We are driven by innovation, committed to performance, and focused on delivering excellence through our people.


Role Overview:

As a Senior Clinical Data Coordinator (CDC II / Senior CDC), you will support core data management activities to ensure accurate, complete, and consistent clinical databases. Working under minimal supervision, your responsibilities will align with global standards including GCP, ICH guidelines, and ICON SOPs. This is an office-based role in Chennai for immediate joiners only.


Key Responsibilities:

  • Ensure compliance with ICON SOPs, GCP, ICH Guidelines, and applicable regulations.

  • Complete all required training, including system-specific and study-related modules.

  • Review CRF/eCRF data for completeness, accuracy, and consistency through computerized and manual checks.

  • Perform external data reconciliation and Serious Adverse Event (SAE) reconciliation.

  • Generate, resolve, and close data queries appropriately.

  • Freeze and/or lock eCRFs in the Electronic Data Capture (EDC) system.

  • Maintain study documentation and files.

  • Conduct User Acceptance Testing and collaborate with CDMS to resolve issues.

  • Handle other project activities like filing, archiving, and query dispatch to investigator sites.

  • Maintain clear and effective communication with the Study Lead, Project Lead, and Project Manager.

  • Log all time in the appropriate timesheet system (e.g., Planview™).


Qualifications and Experience:

  • Bachelor’s degree in a related field.

  • 3–5 years of experience in Core Data Management (DM) activities.

  • Strong understanding of clinical data standards and systems.

  • Ability to work independently while adhering to timelines and quality standards.


Why Join ICON:

ICON’s success is driven by its people. We reward high performance and invest in your growth and well-being with:

  • Competitive salary and annual leave entitlements

  • Customizable health insurance options for you and your family

  • Retirement planning offerings for long-term financial security

  • Life assurance

  • Access to TELUS Health – 24/7 global Employee Assistance Programme

  • Optional benefits such as childcare vouchers, gym memberships, travel passes, health assessments, and more

Explore more benefits here: ICON Careers Benefits


Diversity & Inclusion:

ICON is an equal opportunity employer committed to diversity, inclusion, and accessibility. We welcome all applicants and provide reasonable accommodations where needed. Learn more or request support: ICON Accommodations

Not sure if you meet all the requirements? Apply anyway – you might be exactly what we need!