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Clinical Trial Associate (Cta)

0-2 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

Clinical Trial Associate (CTA) – ICON plc

Location: Montreal, Burlington (Remote)
Job ID: JR136802
Portfolio: Clinical Research In-Home Services, Early Phase Services – ICON Strategic Solutions
Work Type: Remote


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 Clinical Trial Associate (CTA) supports the management and execution of clinical trials by handling a range of administrative and operational tasks. The CTA ensures smooth trial execution through efficient coordination, documentation, and communication with stakeholders across multiple affiliates within the Clinical Development Center (CDC).


Key Responsibilities

Trial Documentation & eTMF Management:

  • Oversight of all trial documentation for assigned clinical trials across adjacent affiliates.

  • Support affiliates in Health Authority (HA) and Ethics Committee (EC) submissions.

  • Ensure compliance with local requirements and electronic Trial Master File (eTMF) processes.

  • Timely uploading, archiving, and compliance checks of trial documents in electronic systems.

  • Provide investigator TMF set-up and core input.

  • Drive consistency in eTMF handling across CDC adjacent affiliate countries.

Administrative & Operational Support:

  • Support and track trial-related payments, including invoice processing for investigator fees.

  • Organize local meetings and coordinate with internal and external stakeholders.

  • Support local safety reporting to Principal Investigators (PIs) and HAs as relevant.

  • Assist in clinical supplies management and tracking.

  • Act as super user for relevant electronic systems and perform other administrative tasks as needed.

Collaboration:

  • Work closely with CDC, local clinical teams, and cross-functional roles including Clinical, Medical, and Regulatory Affairs.

  • Ensure successful planning and conduct of clinical trials within assigned countries.


Required Education & Experience

  • Education: Bachelor’s degree in a scientific or healthcare-related field (highly preferred).

  • Prior experience or strong interest in clinical research.

  • Knowledge of clinical trial processes, regulations, and guidelines.


Skills & Competencies

  • Excellent organizational and communication skills.

  • Ability to work collaboratively in a fast-paced environment.

  • Attention to detail and strong administrative abilities.

  • Ability to coordinate across multiple teams and stakeholders.


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.