Associate Director Quality Management

IQVIA

Kirkland

Sur place

CAD 140 000 - 190 000

Plein temps

Il y a 7 jours
Soyez parmi les premiers à postuler

Une candidature complète en une minute

Un CV et une lettre de motivation personnalisés, prêts à envoyer.

Passez les filtres ATS

Résumé du poste

IQVIA is seeking a Regional Clinical Compliance Lead to guide a cross-country team in delivering compliant, quality-driven clinical operations. You will oversee risk-based activities, CAPA processes, audits, and performance metrics while aligning with global compliance strategies.

Ideal candidate has 8+ years in clinical operations with strong GCP knowledge, leadership experience, and ability to travel across regions to ensure consistent high-quality execution and continuous improvement.

Qualifications

  • Bachelor’s degree in a scientific, medical or healthcare discipline with 8+ years in clinical operations and 4+ years of people management.
  • Minimum 6 years in a GCP compliance or equivalent role; oncology experience preferred.
  • Deep knowledge of ICH, GCP, SOPs and regulatory quality management.
  • Excellent organizational, interpersonal and communication skills; ability to travel.

Responsabilités

  • Lead and develop Regional Clinical Compliance team across multiple countries.
  • Provide expert guidance on regulations and internal standards.
  • Oversee inspections preparation, execution, and follow-up.
  • Ensure CAPA quality and effectiveness; drive standardization.
  • Monitor KPIs, quality metrics, and risk-based compliance activities.

Connaissances

Leadership
Regulatory knowledge
Analytical skills
Communication
Stakeholder management
Problem solving
Team management
Travel readiness
Matrix environment
Quality management

Formation

Bachelor’s degree in scientific/medical/healthcare field
8+ years clinical operations experience
6+ years in GCP/compliance
4+ years people management

Description du poste

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.

Obtenez votre examen gratuit et confidentiel de votre CV.

ou faites glisser et déposez votre fichier ici.

Similar jobs

Postes similaires à comparer

Associate Director Quality Management
Associate Director Quality Management

IQVIA • Quebec

Sur place
CAD 110 000 - 170 000
Clinical FSP Quality Manager
Clinical FSP Quality Manager

IQVIA • Kirkland

Sur place
CAD 90 000 - 130 000
Regional Clinical Compliance Director
Regional Clinical Compliance Director

IQVIA Inc • Quebec

Sur place
CAD 110 000 - 170 000
Regional Clinical Quality & Compliance Director
Regional Clinical Quality & Compliance Director

IQVIA • Kirkland

Sur place
CAD 140 000 - 190 000
Senior Manager, Clinical Quality Assurance
Senior Manager, Clinical Quality Assurance

AbbVie Inc. • Quebec

Sur place
CAD 120 000 - 160 000
Manager, Quality Assurance
Manager, Quality Assurance

NWRPros • Vancouver

Hybride
CAD 135 000 - 185 000
Clinical Research Associate I
Clinical Research Associate I

AbbVie Inc. • Edmonton

Sur place
CAD 65 000 - 90 000
Professional development
Paid time off
Wellness spending account
+2
Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)
Regulatory Affairs Consultant - Process & Compliance (Veeva Quality Document Management SME)

Jobgether • Canada

À distance
CAD 110 000 - 160 000
Flexible remote working environment
Health, vision, and dental insurance
401(k) style retirement plan where/if/
+1
Associate Director, Clinical Supply Management (UK/EU)
Associate Director, Clinical Supply Management (UK/EU)

Summittherapeutics • Town of Oxford

Sur place
CAD 117 000 - 138 000
Associé(e) de recherche clinique (ARC) principal(e)or Attaché(e) de recherche clinique II / Senior Clinical Research Associate or CRA 2
Associé(e) de recherche clinique (ARC) principal(e)or Attaché(e) de recherche clinique II / Senior Clinical Research Associate or CRA 2

IQVIA Inc • Kirkland

Sur place
CAD 70 000 - 97 000