Find Associate director systems Jobs in Dublin 12, D

Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection
IQVIA —Dublin, County Dublin
- Full-time
- Remote
- English
- Microsoft Office
- Bachelor's degree
- Work from home
6d
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Jazz Pharmaceuticals —Dublin, County Dublin
- Engineering
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- Annual leave
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Cushman & Wakefield —DUBLIN 2, County Dublin
- Full-time
- English
- Microsoft Office
- Business development
Quick apply
Senior Area Manager, Ireland - Tommy Hilfiger & Calvin Klein
Tommy Hilfiger —Dublin, County Dublin
- Full-time
Senior Structural Engineer / Associate Designate
Malone O'Regan —Dublin, County Dublin
- Analysis skills
- Budgeting
- Communication skills
Quality Operations Lead
Perrigo —DUBLIN 2, County Dublin
- Hybrid work
- Master's degree
Aseptic Product Quality Associate Director
AbbVie —Dublin, County Dublin
- Full-time
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- Manufacturing
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3h
Associate Director - Protection & Control (P&C) Design Engineer
Jacobs —Dublin, County Dublin
- Hybrid work
- Master's degree
- Bachelor's degree
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12d
Senior fire safety engineer
Marker Group —Dublin, County Dublin
- €60,000–€85,000 a year
- Full-time
- Engineering
- Master's degree
- Analysis skills
Quick apply
7d
Senior Manager, Financial Planning & Analysis
MongoDB —Dublin, County Dublin
- Hybrid work
- Google Suite
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7d
Associate Electrical Engineer
IN2 Design Partnership Ltd —Ranelagh, County Dublin
- €75,000–€80,000 a year
- Full-time
- AutoCAD
- Master's degree
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Quick apply
12d
Associate Director - HV Cable System Design Engineer
Jacobs —Dublin, County Dublin
- Hybrid work
- Engineering
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- No degree
12d
Associate Electrical Director: Data Centres
AECOM —Dublin, County Dublin
- Full-time
- Business development
- In-person
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13d
CNM2; Clinical Trials Research Nurse; Oncology
Beacon Hospital —Dublin, County Dublin
- Full-time
- Management
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- Microsoft Office
- Annual leave
Quick apply
13d
CRM Developer
Glen Dimplex Group —Cloghran, County Dublin
- Full-time
- Azure
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Associate/Senior Quantity Surveyor (MEP) - Data Centres
Mitchell McDermott —Dublin, County Dublin
- Full-time
- Electrical experience
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Quick apply
CRM Developer
Glen Dimplex Europe Holdings Ltd —Cloghran, County Dublin
- Full-time
- Azure
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- Computer Science
Quick apply
Head of Design - Decarbonisation
Alternative Heat —Santry, County Dublin
- Full-time
- No degree
Quick apply
Senior Associate, IT, Network Engineer (Fixed Term Contract - 12 Month)
MUFG Investor Services —Dublin, County Dublin
- Full-time
- Azure
- Computer Science
- AWS
Quick apply

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Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection

IQVIA -
Dublin, County Dublin

Apply Now

Job details

Full-time
6 days ago

Benefits

Work from home

Qualifications

English
Microsoft Office
Bachelor's degree
Continuous improvement
Organisational skills
Computer skills
Leadership
Communication skills
Negotiation

Full job description

Dublin, Ireland | Full time | Home-based | R1559367

General Description:

The Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection is responsible for driving proactive risk management, sustained inspection readiness, audit support, and regulatory compliance across clinical trials. The role provides leadership and oversight to ensure consistent implementation of GCP and regulatory requirements, effective inspection readiness programs, and successful management of inspections and audits.

Key responsibilities include leading inspection readiness and audit support activities at regional or global levels, guiding clinical teams on inspection expectations, coordinating audit and inspection responses, and ensuring timely, high-quality, and compliant remediation. The role also drives a proactive inspection/audit readiness culture, to effectively manage complex, high-risk inspections while maintaining continuous readiness.

Inspection readiness implementation and oversight
• Organize briefing materials, logistics, and stakeholder alignment
• Support inspection readiness across the EMEA region
• Support implementation of standards, tools, and best practices
• Ensure teams are inspection-ready through training and guidance
• Assess inspection risks and oversee mitigation plans
• Supports mock inspections and readiness assessments
• Maintain inspection-ready documentation, processes, and systems
• Supports development of story boards based on global story boards templates and structure and acting as subject matter expert (SME) in content generation together with the relevant functional area SMEs

Inspection and Audit Preparation, Execution and Follow up
• Support regional preparation activities for regulatory inspections and internal/external audits
• Coordinate cross-functional stakeholders (Clinical Operations, QA, country teams)
• Align with Regional Clinical Compliance Lead to conduct targeted site preparation visits as required

Post-Inspection/Audit Activities
• Lead and coordinate responses to inspection/audit findings
• Manage CAPAs, including risk assessment, root cause analysis, and effectiveness checks
• Track CAPAs to timely and effective closure
• Ensure robust root cause analysis and sustainable corrective actions
• Oversee CAPA strategies and regulatory commitments
• Drive consistent, high-quality organizational responses
• Monitor trends and identify opportunities for continuous improvement

Core Competencies, Knowledge and Skill Requirements:

• Understanding of clinical trial processes with a thorough knowledge of ICH-GCP and associated regulatory guidelines
• Analytical and problem-solving skills and high attention to detail, and quality orientation
• Excellent communication and stakeholder management skills
• Influence senior stakeholders and decision-making

Communication & Interpersonal Skills:
• Excellent English written and verbal communication and interpersonal skills
• Excellent organizational skills and ability to prioritize and multi-task
• Ability to work independently in multi-cultural setting and effectively handle multiple priorities in a fast-paced environment

Qualifications
Bachelor’s degree (BS/BA or equivalent) or higher in a scientific, medical or healthcare discipline* with 10+ years in clinical research, clinical operations, or compliance.
Minimum 4 years’** experience in a GCP compliance or equivalent role* (i.e. quality) is preferred.

• Experience in CAPA development and tracking
• Experience in inspections and audits management, including mock inspections and mock interviews
• Deep knowledge of ICH-GCP, regulatory requirements and Clinical trial processes end-to-end
• Experience in oncology global trials is preferred
• Requires deep knowledge of one or more related job areas typically obtained through advanced education combined with experience.
• Sound working knowledge of relevant terminology, International Conference on Harmonization (ICH), Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), applicable regulatory requirements, quality management processes.
• Excellent organizational, interpersonal and communication skills.
• Excellent judgement and decision-making skills.
• Demonstrated leadership and line management skills.
• Excellent influencing and negotiation skills.
• Strong computer skills including Microsoft Office applications.
• Excellent problem-solving skills.
• Demonstrated ability to work in a matrix environment.
• Ability to lead and motivate a clinical team also required.
• Ability to travel within the region/country.
• Ability to establish and maintain effective working relationships with co-workers, managers and clients.
• Fluent in English.

Please note: this role is not eligible for the UK VISA sponsorship.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

associate director systems jobs in dublin 12, d

Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection

Analyst, Corporate Banking, Dublin

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Senior Area Manager, Ireland - Tommy Hilfiger & Calvin Klein

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Associate Director - HV Cable System Design Engineer

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Senior Associate, IT, Network Engineer (Fixed Term Contract - 12 Month)

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