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About the Role

Lead and develop a high-performing team responsible for delivering complex global clinical studies and programs. This role provides strategic and operational oversight across active and pipeline studies, ensuring delivery excellence in timeline, quality, and financial performance. Act as a senior escalation point for sponsors and internal stakeholders, driving resourcing strategy, risk management, governance, and sponsor engagement across key biotech accounts. Play a critical leadership role in talent development, client satisfaction, and business growth, including bid defence support and study award transitions.

Responsibilities

Lead, coach, and develop a team of Clinical Project Management professionals, fostering a high-performance culture.
Manage performance, career development, and succession planning aligned to organisational goals.
Recruit, develop, and retain top talent within a global environment.
Provide ongoing mentoring in project planning, risk management, and problem-solving.
Oversee execution of multiple complex clinical studies/programs to ensure delivery on time, within budget, and to quality standards.
Act as primary escalation point for sponsors and internal stakeholders.
Drive portfolio-level governance, ensuring robust oversight of risk, issues, and financial performance.
Lead resourcing strategy across Project Manager (PM) and Clinical Trial Manager (CTM) teams.
Ensure adherence to SOPs, GCP/ICH guidelines, and regulatory requirements.
Maintain accountability for study budgets, forecasting (EAC), and change control processes.
Review project performance dashboards and ensure accuracy of reporting systems.
Drive strong financial outcomes and proactively manage risks to profitability.
Build and maintain strong relationships with key biotech sponsors.
Support business development activities, including bid defence and proposal development.
Ensure high levels of customer satisfaction and confidence across all engagements.
Navigate complex stakeholder discussions and negotiate effective solutions.
Identify and manage risks across projects, resources, and teams.
Oversee quality issues and implement corrective and preventative actions (CAPA).
Ensure compliance with all regulatory and organisational standards.
Lead or contribute to cross-functional initiatives and process improvements.
Act as a change agent within the organisation, driving adoption of tools and best practices.
Collaborate across global teams, ensuring alignment and knowledge sharing.

Requirements

Bachelor’s degree in Life Sciences or related discipline.
12+ years of relevant experience, including significant clinical project management and leadership experience.
Demonstrated success in managing global clinical trial teams and complex programs.

Skills

Deep knowledge of clinical trial processes and regulatory frameworks (GCP, ICH).
Strong understanding of the clinical research industry and operating environments.
Proven ability to lead through others in a matrixed, global environment.
Strong coaching, mentoring, and team development capabilities.
Ability to manage competing priorities and make sound decisions.
Excellent stakeholder management, influencing, and negotiation skills.
Ability to manage high-stakes client relationships and complex discussions.
Strong financial management capabilities (budgeting, forecasting, change control).
High level of organisational, analytical, and problem-solving skills.
Excellent verbal and written communication skills.
Ability to work effectively across cultures and geographies.
Proficiency in MS Office and clinical project management systems.

Experience Level

12+ years of relevant experience
significant clinical project management and leadership experience

Education Level

Bachelor’s degree in Life Sciences or related discipline

About the Company

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.
We create connections that accelerate the development and commercialization of innovative medical treatments.
Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact.
No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Equal Opportunity

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.