Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
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.