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Configuration & Qc Specialist I

Icon Plc
ICON PLC
1+ years
Not Disclosed
10 Jan. 22, 2026
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

Job Title: Configuration & QC Specialist I – Bangalore
Location: Bangalore, Karnataka, India
Employment Type: Full-time
Work Mode: Office with Flex
Job ID: JR140312


About ICON

ICON plc is a global leader in healthcare intelligence and clinical research, committed to delivering innovative clinical solutions with excellence. We foster an inclusive and collaborative environment, supporting career growth while advancing clinical development and improving patient outcomes.


Role Overview

ICON is hiring a Configuration & QC Specialist I to play a key role in the design, configuration, and quality control of clinical trial databases and systems. This role ensures accurate data capture, system functionality, and regulatory compliance throughout the clinical trial lifecycle.


Key Responsibilities

  • Assist in configuration and setup of clinical trial databases and electronic data capture (EDC) systems in line with project specifications.

  • Perform quality control (QC) checks on clinical trial data and study documentation to identify discrepancies and data entry errors.

  • Collaborate with cross-functional teams, including data management, biostatistics, and clinical operations, to resolve QC findings and ensure data integrity.

  • Support the development and implementation of validation plans to assess the performance of EDC systems and data management processes.

  • Provide training and guidance to end-users on system configuration, data entry procedures, and QC processes to promote compliance and efficiency.


Candidate Profile

  • Bachelor’s degree in Life Sciences, Computer Science, or related field; advanced degree preferred.

  • 1+ years of experience in clinical data management, data entry, or related roles in pharmaceutical or biotechnology settings.

  • Familiarity with clinical trial databases and EDC systems such as Medidata Rave, Oracle Clinical, or Inform.

  • Strong attention to detail, analytical skills, and ability to identify and resolve data-related issues.

  • Excellent communication and interpersonal skills, capable of working effectively in a team-oriented environment.

  • Proactive, adaptable, and eager to learn evolving technologies and processes.


Why Join ICON

  • Global Impact: Contribute to meaningful clinical trials and innovative treatments.

  • Career Growth: Training, mentorship, and skill development opportunities.

  • Comprehensive Benefits: Health insurance, retirement planning, flexible work options, life assurance, wellness programs.

  • Inclusive Culture: ICON fosters diversity, equity, and belonging, promoting a supportive workplace environment.