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Lab Report Coordinator I

Icon Plc
ICON PLC
3+ 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: Lab Report Coordinator I
Location: Bangalore, India
Company: ICON plc
Employment Type: Full-Time | Office-Based (Non-Flex)
Shift Timing: 3 PM – 12 AM

About the Role:
ICON plc, a global leader in healthcare intelligence and clinical research, is seeking a detail-oriented Lab Report Coordinator I to join our team in Bangalore. This role is critical in ensuring timely, accurate, and compliant laboratory reporting for clinical research studies. The Lab Report Coordinator will collaborate with laboratory staff and cross-functional teams to maintain high-quality standards throughout the reporting process.

Key Responsibilities:

  • Coordinate the preparation, formatting, and distribution of laboratory reports according to established protocols and quality standards.

  • Review laboratory reports for accuracy, completeness, and compliance with internal guidelines and regulatory requirements.

  • Collaborate with laboratory teams and cross-functional stakeholders to gather necessary data for report generation.

  • Maintain accurate records of report submissions, distributions, and any required follow-ups or corrections.

  • Support the development and implementation of reporting processes to enhance efficiency, quality, and compliance.

Required Experience & Skills:

  • Bachelor’s degree in Medical Laboratory Technology (MLT).

  • Minimum 3 years of experience in laboratory report coordination, data management, or a related role within a clinical or laboratory setting.

  • Strong attention to detail and organizational skills, with the ability to manage multiple tasks and meet deadlines.

  • Excellent communication and collaboration skills.

  • Proficiency in Microsoft Office Suite; familiarity with Laboratory Information Management Systems (LIMS) is a plus.

Core Competencies:

  • Laboratory report management and data coordination

  • Regulatory compliance and quality assurance

  • Process improvement and documentation accuracy

  • Collaboration and stakeholder communication

Why Join ICON:

  • Be part of a global organization dedicated to shaping the future of clinical research.

  • Competitive salary and comprehensive benefits, including health insurance, retirement planning, life assurance, and wellness programs.

  • Inclusive work environment fostering diversity, growth, and professional development.

  • Opportunities to contribute to high-impact clinical research projects and continuous process improvements.