Director, Clinical Project Management

IQVIA Argentina; Singapore; On-site; SGD 180,000 - 260,000; Full time

Job summary

IQVIA is seeking an experienced Global Project Leader for Oncology to drive end-to-end management of complex, multinational clinical studies. The role involves leading cross-functional teams, managing timelines and budgets, and maintaining strong sponsor relationships across regions including China, the US, and Europe.

Fluency in English and Mandarin is required to engage with global stakeholders. The ideal candidate has 10+ years in project management within CRO/pharma/biotech and a proven

Qualifications

• 10+ years of project management experience in CRO/pharma/biotech.
• Proven track record leading global clinical projects/programs.
• Strong oncology clinical trial experience required.
• Fluent in English and Mandarin.

Responsibilities

• Lead 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.

Skills

Project leadership

Oncology trials

MRCT leadership

English & 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.