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Clinical System Designer

Icon Plc
ICON PLC
5+ 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: Clinical System Designer I – ICON India
Location: Bangalore, India
Employment Type: Full-time
Work Mode: Office with Flex
Job ID: JR141776
Application Deadline: January 23, 2026


About ICON

ICON plc is a world-leading clinical research and healthcare intelligence organization, committed to driving innovation and excellence. Our teams enable the development and delivery of safe and effective therapies globally, while fostering professional growth and a culture of inclusion.


Role Overview

ICON is seeking a Clinical System Designer I to assist in the design, implementation, and optimization of clinical systems that support data collection and management for clinical trials. You will ensure that clinical systems meet user needs, comply with regulatory standards, and contribute to efficient trial operations.


Key Responsibilities

  • Interpret clinical protocols and customer requirements to design clinical data management systems (CDMS) and eCRF components.

  • Develop and configure Custom CRF screens, Edit Checks, and Dynamic Checks, ensuring alignment with ICON/client standards.

  • Collaborate with project teams and serve as a first point of contact for system design queries during study build.

  • Conduct quality control reviews of database specifications and maintain documentation for approvals.

  • Support study kick-offs, review meetings, and change management for post-production system updates.

  • Track and report study-related metrics, meeting minutes, issues, and escalations.

  • Assist team members, embrace process improvement, and contribute to a culture of operational excellence.

  • Travel up to 10% domestically or internationally as required.


Candidate Profile

  • Bachelor’s degree or equivalent in Life Sciences, Computer Science, or related field.

  • 5+ years of experience in clinical systems, data management, or related roles (or equivalent combination of education and experience).

  • Hands-on knowledge of at least one clinical data management system (CDMS) and CRF design tools.

  • Strong problem-solving, analytical, and communication skills.

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

  • Familiarity with regulatory standards and compliance requirements.


Why Join ICON

  • Global Impact: Contribute to international clinical trials and innovation in healthcare.

  • Career Growth: Access mentorship, skill development, and opportunities to advance within clinical system design and data management tracks.

  • Comprehensive Benefits: Competitive salary, health insurance, retirement plans, flexible work options, and wellness programs.

  • Inclusive Culture: ICON values diversity, equity, and belonging, creating a supportive and collaborative workplace.