Clinical Documentation Coordinator I

ICON; Cow Ark; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading clinical research organization is seeking a Clinical Data Coordinator I. This role is crucial for managing clinical and lab data while ensuring compliance with protocols. Candidates should have a Bachelor's degree and at least one year of experience in clinical or lab data review. ICON offers a competitive salary and benefits that promote work-life balance. Join us to contribute to innovative research in a supportive environment.

Benefits

Various annual leave entitlements

Health insurance options

Retirement planning options

Global Employee Assistance Programme

Life assurance

Flexible country-specific benefits

Qualifications

• At least 1 year of clinical or lab data review experience.
• Experience in Oncology and/or Inflammatory therapeutic areas preferred.
• Ability to cross-check information with protocols.

Responsibilities

• Receive local laboratory information and transcribe into EDC system.
• Crosscheck information with protocols to ensure completeness.
• Collaborate with team members to resolve documentation issues.

Skills

Clinical data review

Collaboration with CDMs and CRAs

Data transcription into EDC systems

Attention to detail

Education

Bachelor’s Degree in clinical research or related field

Tools

Electronic Data Capture (EDC) systems

Job description

As a Clinical Data Coordinator I, you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.

What you will be doing:

• Receive relevant local laboratory information from investigative sites and transcribe this into the EDC system or into a template for import.
• Crosscheck information with the protocol to ensure all required analytes are accounted for.
• Collaborate with Clinical Data Managers (CDMs), Clinical Research Associates (CRAs), and investigative sites to clarify source documentation issues and obtain updates.
• Attend Clinical Data Management group meetings and departmental trainings regularly.
• Perform other duties as assigned.

You are:

• Bachelor’s Degree or equivalent experience in clinical research or a related field.
• At least 1 year of clinical or lab data review experience, including reviewing lab/analyte data or source documentation.
• Experience with Electronic Data Capture (EDC) systems preferred.
• Experience in Oncology and/or Inflammatory therapeutic areas preferred.

What ICON can offer you:

Our success depends on the quality of our people. We prioritize building a diverse culture that rewards high performance and nurtures talent.

In addition to a competitive salary, ICON offers a range of benefits focused on well-being and work-life balance, including:

• Various annual leave entitlements
• Health insurance options for you and your family
• Retirement planning options
• Global Employee Assistance Programme with TELUS Health
• Life assurance
• Flexible country-specific benefits such as childcare vouchers, gym memberships, travel passes, and health assessments

Visit our careers website to learn more: https://careers.iconplc.com/benefits

ICON values inclusion & belonging, providing an accessible environment for all candidates. We are committed to equal opportunity employment. If you require reasonable accommodation during the application process, please inform us through this form.

Interested but unsure if you meet all requirements? We encourage you to apply — you might be exactly who we’re looking for.

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