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Cra Ii/Senior Cra

1+ years
Not Disclosed
10 Oct. 13, 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

CRA II / Senior Clinical Research Associate (CRA) – ICON plc

Location: Blue Bell, US (Remote, Office or Home)
Job ID: JR134544
Portfolio: Clinical Monitoring – ICON Full Service & Corporate Support
Work Type: Remote / Office


Company Overview

ICON plc is a global leader in healthcare intelligence and clinical research. The organization fosters an inclusive environment that drives innovation and excellence, aiming to shape the future of clinical development.


Role Overview

The CRA II / Senior CRA is responsible for monitoring and managing clinical trial sites, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. The role focuses on maintaining data integrity, participant safety, and smooth trial execution across multiple sites.


Key Responsibilities

Site Monitoring & Management:

  • Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and GCP standards.

  • Conduct site visits to assess performance, resolve issues, and support trial execution.

  • Provide training and guidance to site staff and other CRAs to maintain clinical quality standards.

  • Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

  • Collaborate with cross-functional teams to ensure accurate and timely data collection and reporting.

Project Oversight:

  • Manage multiple sites and projects simultaneously.

  • Ensure compliance with monitoring practices and data integrity requirements.

  • Influence site adherence and drive compliance within a complex clinical environment.


Required Education & Experience

  • Advanced degree in Life Sciences, Nursing, or Medicine.

  • Extensive experience as a Clinical Research Associate (CRA).

  • Minimum of 12 months of independent monitoring experience.

  • Strong knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

  • Proficiency in relevant clinical trial software and tools.

  • Experience managing multiple sites and projects concurrently.

Location Requirement:

  • Candidates should be located in Central, West, or East regions of the US.


Skills & Competencies

  • Excellent organizational, problem-solving, and analytical skills.

  • Strong communication, interpersonal, and stakeholder management abilities.

  • Ability to build and maintain professional relationships with site personnel.

  • Ability to work independently in a remote environment while contributing to team goals.


Benefits

ICON offers competitive compensation along with a comprehensive benefits package designed to promote well-being and work-life balance:

  • Various annual leave entitlements

  • Health insurance options for employees and families

  • Competitive retirement planning offerings

  • Global Employee Assistance Programme (LifeWorks – 24/7 access to specialized professionals)

  • Life assurance

  • Flexible, region-specific optional benefits (childcare vouchers, gym memberships, bike purchase schemes, subsidized travel passes, health assessments, etc.)

More details: ICON Careers Benefits


Diversity & Inclusion

ICON is committed to inclusion, belonging, and providing a workplace free of discrimination and harassment. All candidates receive equal consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Reasonable accommodations are available: Request here


Application Encouragement

Candidates are encouraged to apply even if they do not meet all requirements, as they may still be a strong fit for this or other ICON roles.