Director, Clinical Project Management

IQVIA; Singapore; On-site; SGD 180,000 - 300,000; Full time

Job summary

IQVIA is seeking a seasoned Global Project Leader for Oncology to drive end-to-end delivery of complex multinational studies. You will lead cross-functional teams across regions, manage timelines and budgets, and serve as the main client contact to ensure satisfaction and strategic alignment.

The role requires 10+ years in project management within CRO/pharma/biotech, with 7+ years leading global clinical programs and strong oncology trial experience. English and Mandarin fluency are essential.

Qualifications

• 10+ years of project management experience in CRO/pharma/biotech.
• 7+ years leading global clinical projects/programs independently.
• Strong oncology clinical trial experience required.
• Proven Project Lead for MRCTs in a global/multi-regional setting.
• Fluent in English and Mandarin.

Responsibilities

• Lead end-to-end delivery of complex global oncology studies ensuring quality, timelines, budgets, and client satisfaction.
• Serve as primary sponsor and stakeholder contact, managing expectations throughout the project lifecycle.
• Drive cross-functional global teams to milestones, mitigate risks, and resolve operational challenges.
• Lead complex multinational and multi-regional clinical trials (MRCTs) across regions including China, the US, and Europe.
• Influence and drive results across a global matrix organization without direct reporting authority.
• Support business development activities, including RFP responses, bid defenses, client presentations, and strategic account growth initiatives.
• Partner with sponsors to understand development strategies and deliver tailored project solutions.
• Contribute to client retention, expansion, and new business opportunities.

Skills

Project management

Global/multinational trials

Oncology trials

Leadership

Client/stakeholder management

English and Mandarin

Job description

Global Project Leadership Team (Oncology) Key Responsibilities

• Lead the end-to-end delivery of complex global oncology clinical studies and programs, ensuring quality, timelines, budgets, and customer satisfaction.
• Serve as the primary point of contact for sponsors and stakeholders, building strong client relationships and managing expectations throughout the project lifecycle.
• Drive cross-functional global teams to achieve study milestones, proactively identify and mitigate risks, and resolve operational challenges.
• Lead complex multinational and multi-regional clinical trials (MRCTs), ensuring successful execution across regions including China, the US, and Europe.
• Influence and drive results across a global matrix organization without direct reporting authority.
• Support business development activities, including RFP responses, bid defenses, client presentations, and strategic account growth initiatives.
• Partner with sponsors to understand development strategies and deliver tailored project solutions.
• Contribute to client retention, expansion, and new business opportunities .

Requirements

• 10+ years of project management experience within CRO, pharmaceutical, or biotechnology organizations, including 7+ years independently leading global clinical projects/programs .
• Strong oncology clinical trial experience is required.
• Proven track record serving as a Project Lead (PL) for complex global and multi-regional clinical studies (MRCTs).
• Fluent in English and Mandarin .

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.