Project Manager
Talent Acquisition Team Lead
- Icon Strategic Solutions
About the role
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At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.
Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
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?
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.
Benefits of Working in ICON :
Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.
#LI-APAC2
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
12/10/2025
Summary
Zhong Yao's Journey at ICON Plc in China Zhong Yao's career in clinical research spans over two decades, with leadership roles across major CROs and a commitment to advancing healthcare in China.
Teaser label
IndustryContent type
BlogsPublish date
12/01/2025
Summary
How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i
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IndustryContent type
BlogsPublish date
11/28/2025
Summary
Quality and Compliance for New Entrants: A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job
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