Operational Compliance Associate II (Part-Time, Home-Based with UK Travel)

Operational Compliance Associate II (Part-Time, Home-Based with UK Travel)

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Company: ICON plc
Location: Home-based (Regular UK Travel Required)
Job Type: Part-Time
Department: Quality Assurance
Application Deadline: Open until filled
Salary: Competitive
Benefits: Extensive (detailed below)

About ICON plc

ICON plc is a global leader in healthcare intelligence and clinical research. Our mission is to drive innovation and excellence within the clinical development sector. We pride ourselves on creating an inclusive environment that fosters creativity and collaboration. Join us as we continue to shape the future of clinical research.

Job Overview

We are seeking an Operational Compliance Associate II to join our dynamic team. This role involves working within the Quality Department under the supervision of the Senior Manager, Quality Assurance. As part of our Firecrest Clinical team, you will help produce highly visual and engaging products for the Clinical Trial Industry, contributing to the improvement of site performance and adherence to industry standards.

Key Responsibilities

• Operational Quality Framework: Implement and execute quality checks on clinical documentation at Accellacare investigator sites.
• Quality Issues Management: Facilitate root cause analysis sessions and support the development of Corrective and Preventive Actions (CAPA).
• Data Metrics: Collate and report metrics on quality data to management.
• Audit Support: Track and support client audits and regulatory inspections.
• Operational Improvement: Drive quality and process improvements across sites to enhance operational efficiency and compliance.
• Compliance Visits: Perform compliance visits at Accellacare sites to review study data and clinical trial documentation.
• Quality Support: Assist with reporting and investigating quality issues, ensuring adherence to SOPs and regulations.

Qualifications

Requirement	Details
Education	Bachelor’s degree in a Scientific Subject or relevant qualification (Diploma, Certificate).
Experience	Minimum 2 years in clinical research within a Site Management Organisation, Clinical Research Organisation, NHS, Academia, or Pharmaceutical sector.
Knowledge	Working knowledge of GCP guidelines and quality regulations.
Skills	Strong MS Word and Excel skills, excellent communication and interpersonal skills.
Travel	Willingness to travel regionally (approximately 20%).
Personal Attributes	Highly organized, detail-oriented, self-motivated, assertive, flexible, with a focus on quality and customer service.

Why Join ICON?

Our success is built on the quality of our people. At ICON, we foster a diverse culture that rewards high performance and nurtures talent.

Benefits

• Annual Leave: Various entitlements based on location.
• Health Insurance: Tailored health insurance packages to suit your needs.
• Retirement Planning: Competitive retirement plans to help you plan for the future.
• Employee Assistance Program: Access to LifeWorks, a global network of over 80,000 professionals available 24/7 for support.
• Life Assurance: Security for you and your loved ones.
• Flexible Benefits: Country-specific options including childcare vouchers, gym memberships, and more.

For more detailed information about our benefits, visit our careers site.

How to Apply

Interested candidates are encouraged to apply, even if you don’t meet all the requirements. We value diverse skills and experience.

Current ICON Employees: Please apply here.

General Applicants: Submit your application through our careers portal or send your resume to email@example.com.

Reasonable Accommodations: If you require accommodations due to a medical condition or disability, please submit a request.

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