Jobs at IQVIA

The Clinical Trial Assistant supports clinical projects by managing documentation, communicating with teams, and ensuring compliance with regulations.

The Clinical Project Manager oversees clinical trials, managing timelines, budgets, and ensuring regulatory compliance while mentoring junior team members and engaging with clients.

The Account Director manages key client accounts, ensuring satisfaction and growth while collaborating on strategic plans and overseeing project execution.

As an Analyst, you will analyze client requirements, collaborate on data-driven solutions, and deliver insights for healthcare strategies.

Lead and develop a team overseeing global clinical studies, ensuring timelines and quality standards are met while managing risks and financial performance.

The Consultant will manage end-to-end market research projects, apply qualitative and quantitative methodologies, and deliver actionable insights to clients in healthcare.

The Site Activation Specialist will manage site activation, documentation, and coordination between departments while tracking site performance and maintaining contact with investigative sites.

The Senior Contract Associate oversees preparation, negotiation, and finalisation of clinical trial agreements. Responsibilities include contract efficiency, collaboration with stakeholders, and maintaining compliance with regulations.

Lead the Data, Technology, and Advisory Services growth in JAPAC, driving strategy, client engagement, and team development across multiple sectors.

Assist Clinical Research Associates and Regulatory teams with administrative tasks, document management, and communication for clinical trials, ensuring compliance and accuracy.

As Senior Counsel, you'll provide legal advice on M&A, commercial contracts, technology transactions, and regulatory compliance, supporting the legal needs in digital health and life sciences across the APAC region.

The Senior Clinical Research Associate will perform site monitoring and management tasks to ensure compliance with study protocols and regulatory guidelines, manage recruitment plans, and collaborate with study team members for project execution.

The role involves site monitoring, managing study progress, ensuring regulatory compliance, and communicating effectively with sites and project teams.

The Site Activation Specialist (SAS) manages site start-up activities, including ethics submissions, budget negotiations, and communication with internal and external stakeholders to ensure compliant site activation.

The Clinical Research Coordinator supports the execution of clinical trials through administrative tasks, patient enrollment, data management, and communication with study monitors.