Drive employee engagement, performance, and career development.
Conduct Accompanied Site Visits (ASVs) to coach CRAs, strengthen monitoring skills and support high-quality site monitoring.
Support CRA/CTA onboarding and training to build the skills required for their role.
Foster a high-performance culture focused on accountability, collaboration, and continuous improvement.
Participate in new staff recruitment activities, including candidate screening and interviews.
Operational Excellence
Ensure sufficient CRA/CTA resources and skills are available for each project and collaborate with the project team to meet customer and site requirements.
Monitor team performance, productivity, and quality metrics.
Identify operational risks and implement corrective and preventive action plans.
Ensure compliance with all applicable regulatory requirements, GCP, and company procedures.
Develop and implement strategies to achieve project, departmental and business objectives.
Site & Customer Partnership
Contribute to building and maintaining strategic relationships with key research sites and investigators.
Act as a site advocate within IQVIA, supporting improvements in site capability, quality and productivity.
Partner with sponsor representatives and cross-functional teams to achieve study objectives.
Attend customer meetings and maintain ongoing local sponsor partnerships.
Business & Quality Management
Support delivery that meets customer expectations and contributes to business profitability.
Ensure accurate reporting and maintenance of clinical systems and documentation.
Promote innovation and continuous improvement within clinical operations.
Support change management initiatives and implementation of new ways of working.
What You'll Bring
Essential Requirements
Bachelor's Degree in Life Sciences, Healthcare or a related scientific discipline.
Significant experience within clinical research and clinical operations.
Strong practical knowledge of clinical trial conduct, monitoring activities, and research site operations.
Advanced knowledge of ICH GCP guidelines and applicable regulatory requirements.
Excellent communication, organisation, and problem-solving skills.
Demonstrated people leadership, including the ability to coach, mentor, provide constructive feedback and support the development of others.
Ability to collaborate effectively and build strong partnerships with sites, sponsors, and internal stakeholders.
Preferred Requirements
Previous line management experience within a CRO or Sponsor.
Experience supporting or leading CRAs across multiple therapeutic areas.
Exposure to change management and process improvement initiatives.
Why IQVIA?
At IQVIA, you'll join a global leader in clinical research where innovation, collaboration, and professional development are at the heart of everything we do.
We offer
Career progression opportunities within a global organisation
Flexible work arrangements
Exposure to innovative clinical trials and therapies
Comprehensive development and leadership programs
A culture focused on collaboration, inclusion, and continuous learning
Ready to Make an Impact?
If you are passionate about clinical research, people leadership, and delivering operational excellence, we would love to hear from you.
Apply today and help shape the future of clinical research.
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.
