Instagram
youtube
Facebook

Cdc I

1+ years
Not Disclosed
10 April 18, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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 Data Coordinator I (CDC I)


Location:

United States (Remote)


Job ID:

2025-118543


Department:

  • Clinical Data Management

  • Clinical Data Scientist Lead

  • Clinical Systems

  • Data Standards Consultant
    (ICON Strategic Solutions)


Job Type:

Full-Time, Remote


Application Contact:

Name: Brendan Hoey
Message Option: Send a message via job platform
Other Roles: [View other roles by Brendan]


Job Description:

About ICON:
ICON plc is a global leader in clinical research and healthcare intelligence, committed to delivering innovation and quality through a diverse and talented workforce.


Key Responsibilities:

Data Review

  • Conduct data review of clinical trial data, including managing data queries.

  • Perform reconciliation of external data vs. EDC (Electronic Data Capture) data.

  • Assist in running study reports, metrics, and creating study documents.

  • Support review activities during interim and final database locks.

Documentation & Filing

  • File study documentation in the electronic Trial Master File (eTMF).

  • Conduct periodic quality checks on eTMF documents.

  • Support meeting documentation, tracking, data archival, and inspection readiness.

Data Collection Systems

  • Support the setup and testing of study data collection tools.

Quality Support

  • Participate in quality reviews of CRO activities.

  • Ensure personal compliance with training and GxP (Good Practice) standards.

  • Handle other duties as assigned.


Qualifications & Experience:

  • Education: Associate or Bachelor's degree preferred

  • Experience:

    • 1+ year of relevant work experience preferred (or equivalent training/experience)

    • Familiarity with electronic data collection systems

    • Understanding of data management best practices in clinical trials

    • Preferred knowledge of FDA and ICH regulations/standards


ICON Employee Benefits Include:

  • Generous annual leave

  • Customizable health insurance plans

  • Strong retirement savings options

  • 24/7 Global Employee Assistance Programme (TELUS Health)

  • Life assurance

  • Optional benefits (varies by country):
    Childcare vouchers, gym memberships, travel subsidies, bike-to-work schemes, and more

🔗 Learn more about ICON benefits


Diversity & Inclusion Commitment:

ICON is dedicated to creating an inclusive, accessible, and discrimination-free workplace. All qualified candidates are encouraged to apply regardless of background or whether all qualifications are met.