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Cta Base

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ICON
1-3 years
Not Disclosed
10 Dec. 15, 2025
Job Description
Job Type: Full Time Remote 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

Clinical Associate (CTA Base) – Immunology

Location: Remote (USA – Blue Bell, PA preferred)
Category: Clinical Operations / Research & Development
Employment Type: Full-Time
Experience Required: 1–3 years in clinical research or related healthcare setting


About ICON

ICON plc is a global leader in healthcare intelligence and clinical research, dedicated to advancing innovative treatments and therapies. With a commitment to inclusion, diversity, and excellence, ICON fosters an environment where collaboration and innovation drive meaningful impact in clinical development worldwide.


Position Overview

ICON is seeking a Clinical Associate (CTA Base – Immunology) to support clinical trial operations in immunology studies. The Clinical Associate will play a key role in planning, executing, and monitoring clinical trials, ensuring adherence to protocols, regulatory requirements, and industry best practices. This role offers flexibility with remote work while collaborating closely with ICON’s operational teams.


Key Responsibilities

  • Assist in clinical trial planning, site initiation, patient recruitment, and monitoring activities to ensure data quality and compliance.

  • Coordinate trial activities, including data collection, site management, and monitoring visits, maintaining accurate study documentation.

  • Collaborate with cross-functional teams, including Clinical Operations, Data Management, and Biometrics, to ensure timely and efficient trial execution.

  • Support study close-out activities, including data cleaning, analysis, and preparation of clinical study reports.

  • Maintain adherence to GCP, ICH guidelines, and internal SOPs, ensuring regulatory compliance throughout the trial lifecycle.

  • Communicate effectively with study teams and clinical sites to resolve operational or data-related issues.


Required Qualifications

  • Bachelor’s or advanced degree in Life Sciences, Health Sciences, or related field.

  • Minimum 1–3 years of clinical research experience, preferably in pharmaceutical, biotechnology, or CRO settings.

  • Strong organizational and time management skills with the ability to prioritize multiple tasks efficiently.

  • Excellent attention to detail and problem-solving skills to maintain data integrity and compliance.

  • Effective communication and interpersonal skills to collaborate cross-functionally with study teams and clinical sites.

  • Knowledge of clinical trial regulations, GCP, and industry standards is preferred.


Why Join ICON

ICON provides competitive compensation and a comprehensive benefits package designed to support employees’ professional growth, well-being, and work-life balance, including:

  • Generous annual leave and flexible working options

  • Comprehensive health insurance plans for employees and families

  • Competitive retirement planning and 401(k) options

  • Global Employee Assistance Programme (LifeWorks) providing 24/7 support

  • Life assurance and optional country-specific benefits such as childcare vouchers, gym discounts, and health assessments

At ICON, inclusion and belonging are core to our culture. All qualified applicants receive equal consideration for employment regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.


Apply Today

Join ICON to contribute to transformative clinical research in immunology, working in a collaborative, globally connected environment. Candidates with 1–3 years of relevant clinical research experience are encouraged to apply, whether for this position or other opportunities across ICON.