Clinical Operations Leader - Develop Teams & Trials

IQVIA Inc

North Sydney

On-site

AUD 140,000 - 190,000

Full time

2 days ago
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Job summary

IQVIA Inc in Sydney is seeking a Clinical Operations Manager (Line Manager) to lead, develop and inspire a team of CRAs and CTAs, delivering high‑quality clinical research. You’ll coach, monitor performance and align resources with study needs to improve site capability and trial delivery.

You’ll partner with study teams, sponsors and sites to manage risks, ensure GCP compliance and continuous improvement while focusing on talent development, recruitment and building strategic, collaborative

Qualifications

  • Bachelor's Degree in Life Sciences, Healthcare or a related scientific discipline.
  • Significant experience within clinical research and clinical 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.

Responsibilities

  • Lead, coach, mentor, and motivate a team of CRAs and/or CTAs across multiple projects.
  • Drive employee engagement, performance, and career development.
  • Conduct Accompanied Site Visits (ASVs) to coach CRAs and strengthen monitoring skills.
  • 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.

Skills

People leadership
Communication
Organisational skills
Problem-solving
Stakeholder management

Education

Bachelor's Degree in Life Sciences or related discipline

Job description

IQVIA Inc in Sydney is seeking a Clinical Operations Manager (Line Manager) to lead, develop and inspire a team of CRAs and CTAs, delivering high‑quality clinical research. You’ll coach, monitor performance and align resources with study needs to improve site capability and trial delivery.

You’ll partner with study teams, sponsors and sites to manage risks, ensure GCP compliance and continuous improvement while focusing on talent development, recruitment and building strategic, collaborative

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