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Project Manager

JR065090

About the role

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Cross Functional Project Manager - RWE Late Phase Research

Taiwan, HK or China (office or home based)

Are you an experienced Clinical Project Manager, with a solid understanding of Late Phase studies, including preferably management of IIIb, Phase IV and Observational Trials?

ICON PLC, are a leading Clinical Research Organisation with a strong global reputation in our approach to clinical development. We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients. We have offices in 40 countries with around 100 offices worldwide and over 15,000 employees globally.

We're currently looking for experienced cross functional Project Managers across APAC region.

As a Full Services Project Manager, you will be expected to contribute towards a culture of business excellence with a focus on streamlining processes, adding value to the business and exceeding client needs. You will be the primary point of contact for designated projects, responsible for: delivering successful working relationships with clients, cross functional project planning, scheduling and implementation, defining project scope, budget, resource requirements and deliverables, risk migration strategies, associated action plan and issue resolution.

Responsibilities will also include supporting the development of proposals, bid defense presentations, as well as communicating globally both verbally and written, with clients, vendors and others within the organisation, over email, on the phone and face to face. This role will also include management of support staff.

Applicants must be able to demonstrate drive, passion and a strong sense of team working, along with a desire to progress within our organisation.

Successful candidates will have;

* Bachelor's Degree in medicine, science or equivalent;
* Demonstrable Project Management experience within clinical research is essential;
* Strong communication, planning, decision-making, negotiation, conflict management and time management skills;
* Major experience in global/multi-countries late phase studies needed;
* Willingness to travel up as needed

What happens next?

Following your application, your CV will be reviewed and if your profile is suitable, you will be contacted by one of our dedicated recruiters who will be able to provide you with more details about this opportunity.

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Why Francis returned to ICON: building a long-term career in clinical research Francis Kayamba is a Clinical Research Associate based in Johannesburg, South Africa. He first joined ICON in February

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Lydia's Journey Back to ICON

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Publish date

03/24/2026

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