JUMP TO CONTENT

Project Manager

JR071674

About the role

This vacancy has now expired. Please click here to view live vacancies.

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

List #1

Day in the life

Headshot of male
Leading Through Change: Zhong Yao's Journey at ICON in China

Teaser label

Our People

Content type

Blogs

Publish 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

From culture to collaboration, Zhong Yao explains how ICON China delivers quality clinical trials, and empowers local talent.

Read more
Two computer monitors with data graphs
How Data Moves Through a Clinical Trial

Teaser label

Industry

Content type

Blogs

Publish 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

Teaser label

Discover how data flows through a clinical trial and learn where your skills could fit within clinical research.

Read more
Male and female auditing a manufacturing facility
Quality and Compliance - A Plain Language Guide

Teaser label

Industry

Content type

Blogs

Publish 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

Teaser label

A clear, practical introduction to quality and compliance for those starting a career in clinical research.

Read more
View all

Similar jobs at ICON

Clinical Trial Assistance

Salary

Location

Regional United States (PRA)

Location

Multiple US Locations

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Operations

Job Type

Permanent

Description

We are currently seeking a CTA to join our diverse and dynamic team. As a CTA ICON, you will play a pivotal role in supporting the design, implementation, and management of clinical trials, contributi

Reference

JR139998

Expiry date

01/01/0001

Brandon Pupek

Author

Brandon Pupek
Read more Shortlist Save this role
Project Specialist

Salary

Location

Regional United States (PRA)

Location

Multiple US Locations

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Project/ Program Management

Job Type

Permanent

Description

We are currently seeking a Research Operations Coordinator to join our diverse and dynamic team. As a Research Operations Coordinator at ICON, you will play a pivotal role in supporting various projec

Reference

JR141111

Expiry date

01/01/0001

Brandon Pupek

Author

Brandon Pupek
Read more Shortlist Save this role
Pharmacovigilance Systems Specialist

Salary

Location

India, Chennai

Location

Bangalore

Chennai

Trivandrum

Bengaluru

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Drug Safety

Job Type

Permanent

Description

We are currently seeking a Pharmacovigilance Systems Specialist to join our diverse and dynamic team. As a Pharmacovigilance Systems Specialist at ICON, you will be responsible for managing and optimi

Reference

JR136739

Expiry date

01/01/0001

Archana Bakkiyarajan Read more Shortlist Save this role
CDC II

Salary

Location

Mexico, Mexico City

Location

Mexico City

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Data Management

Job Type

Permanent

Description

What you will be doing  Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures.Manage clinical and third-party data reconciliation base

Reference

JR135148

Expiry date

01/01/0001

Daniela Guerrero Read more Shortlist Save this role
Pharmacovigilance Associate - Post Marketing (FSP - Sponsor Dedicated)

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Drug Safety

Job Type

Permanent

Description

We are currently seeking a Pharmacovigilance Associate to join our diverse and dynamic team. As a Pharmacovigilance Associate at ICON, you will play a vital role in monitoring and ensuring the safety

Reference

JR141138

Expiry date

01/01/0001

Simone Chan

Author

Simone Chan
Simone Chan

Author

Simone Chan
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above