Find The associate director, linux/unix systems engineer Jobs in Dublin, D

Associate Director Quality - Client Dedicated ( Regional Clinical Compliance Lead)
IQVIA —Dublin, County Dublin
- Full-time
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- English
- Microsoft Office
- Bachelor's degree
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The Associate Director, Linux/Unix Systems Engineer
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International HEOR & HTA Associate Director, NS
Novartis —Dublin, County Dublin
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Senior Associate, IT, Network Engineer (Fixed Term Contract - 12 Month)
MUFG Investor Services —Dublin, County Dublin
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Associate Director, Regulatory Affairs - Pricing & Underwriting
Optum —Dublin, County Dublin
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Data & AI Consultant – Associate Director - ROI / Belfast
Grant Thornton —Dublin, County Dublin
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Global Labelling Associate Director, Content (Established Products)
Novartis —Dublin, County Dublin
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Associate Director, Industry Relations. Rebate Modeling
Optum —Dublin, County Dublin
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PGIM | Director, Designated Person For Fund Risk (PCF 39C)
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Associate Director, Reporting & Insights Partner R&D & Technical Operations
Jazz Pharmaceuticals —Dublin, County Dublin
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Associate Director, Network Contracting
Optum —Dublin, County Dublin
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Associate Director, Global Publications & Foundational Content
Novartis —Dublin, County Dublin
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Associate Director - Privacy
Grant Thornton —Dublin, County Dublin
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Associate Director, Drug Product Development
Jazz Pharmaceuticals —Dublin, County Dublin
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Associate Director, Business Process
Optum —Dublin, County Dublin
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Global Labelling Associate Director, Content (Oncology)
Novartis —Dublin, County Dublin
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Associate Director, Infrastructure Advisory
Turner & Townsend —Dublin, County Dublin
- Full-time
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Quick apply
10d
PGIM | Director, Designated Person For Fund Risk
Prudential —Dublin, County Dublin
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Associate Director Quality - Client Dedicated ( Regional Clinical Compliance Lead)

IQVIA -
Dublin, County Dublin

Apply Now

Job details

Full-time
4 days ago

Benefits

Work from home

Qualifications

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

Full job description

Dublin, Ireland | Full time | Home-based | R1559343

General Description:

The Regional Clinical Compliance Lead is responsible for leading, developing, and managing a team of Clinical
Compliance professionals supporting country- and site-level oversight. This role combines people leadership with
operational and strategic accountability to ensure consistent, high-quality execution of risk-based compliance
activities.
This role plays a critical role in building team capability, driving performance, and ensuring alignment with global
compliance strategies while fostering a culture of quality, accountability, and continuous improvement.

Essential Functions
• Serve as the primary point of contact for the RCC country compliance managers team regarding: - GCP requirements
- Company and study-specific procedures
- General compliance-related queries
• Provide expert guidance and interpretation of regulations and internal standards to ensure consistent and compliant practices.
• Oversee preparation, execution, and follow-up activities for inspections
• Provide leadership support during high-impact audits and inspections.
• Ensure consistent application of lessons learned across the team.

Operational Oversight & Execution Excellence
• Ensure consistent and high-quality execution of risk-based compliance activities across countries and studies.
• Monitor key performance indicators (KPIs), quality metrics, and compliance trends across the team•
Identify systemic risks, recurring issues, and areas for improvement.
• Ensure timely escalation to Head RCC EMEA and effective resolution of critical compliance issues.• Drive accountability for CAPA quality and effectiveness.
• Provide oversight and quality review of:
- Remote Compliance Activities
- Risk identification and mitigation strategies
- Site-level compliance assessments
- Drive standardization and harmonization of processes across the team.

Resource & Capacity Management
• Manage and oversee the budget, resource allocation and workload balancing across the team based on
study portfolio and risk profile.
• Ensure appropriate resourcing for high-risk studies, sites, and compliance activities.
• Partner with senior leadership on workforce planning and capability needs.

Strategic Alignment & Cross-Functional Partnership
• Translate global compliance strategies into clear team-level objectives and actions.
• Ensure alignment between local execution and global expectations by partnering with:
- RCC Inspection and Audit Lead
- RCC Process Excellence and Risk Surveillance
- Global Clinical Compliance
- Clinical Operations leadership
- Quality Assurance teams
• Represent the function in governance forums and cross-functional discussions.

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
• High attention to detail and quality orientation
• Excellent communication and stakeholder management skills

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

Supervisory Responsibilities:
• Lead, coach, and develop a team of Regional Clinical Compliance professionals across multiple countries.
• Set clear performance expectations and conduct regular performance reviews (goal setting, mid-year,
year-end).
• Build organizational capability by identifying skill gaps and implementing targeted development plans.
• Foster a culture of quality, accountability, continuous improvement, and psychological safety.
• Drive talent management, including succession planning and retention of key talent.
• Promote an inclusive, collaborative, and high-performing team environment aligned with company values.
• Encourage feedback, innovation, and continuous learning.
• Model ethical behavior and reinforce a compliance mindset across the team

Qualifications

•Bachelor’s degree (BS/BA or equivalent) or higher in a scientific, medical or healthcare discipline* with minimum of 8 years of progressive experience in clinical operations roles plus minimum 6 years’ experience in a GCP compliance or equivalent role (i.e. quality) including people management experience (minimum 4 years).
• 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 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

the associate director, linux/unix systems engineer jobs in dublin, d

Associate Director Quality - Client Dedicated ( Regional Clinical Compliance Lead)

The Associate Director, Linux/Unix Systems Engineer

Network Development Engineer , European Sovereign Cloud, ADC Networking International

International HEOR & HTA Associate Director, Oncology

International HEOR & HTA Associate Director, NS

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

Associate Director, Regulatory Affairs - Pricing & Underwriting

Data & AI Consultant – Associate Director - ROI / Belfast

Global Labelling Associate Director, Content (Established Products)

Associate Director, Industry Relations. Rebate Modeling

PGIM | Director, Designated Person For Fund Risk (PCF 39C)

Associate Director, Reporting & Insights Partner R&D & Technical Operations

Associate Director, Network Contracting

Associate Director, Global Publications & Foundational Content

Associate Director - Privacy

Associate Director, Drug Product Development

Associate Director, Business Process

Global Labelling Associate Director, Content (Oncology)

Associate Director, Infrastructure Advisory

PGIM | Director, Designated Person For Fund Risk

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