JUMP TO CONTENT

Project Manager

061387_1573450451

About the role

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

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. ICON Clinical Research is Whole Owned Foreign Company which founded in 1990 in Ireland.

We expanded our business from 1996 in APAC region.

 

Currently we are hiring the Full Services Project Manager in China.

As a Full Services (Senior) 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, resource requirements and deliverables, risk migration strategies, associated action plan and issue resolution.

- Primary point of contact for designated projects and responsible for developing successful working relationship with clients

- Responsible for cross functional project planning, scheduling and implementation of cross functional project(s)

- Define project scope, resource requirements and deliverable

- Responsible for risk mitigation strategies, associated action plan and issue resolution

- Proactively manage any study budget including changes in scope

- Collaborate with Business Development to ensure timely competition of change orders

- Track project deliverables using appropriate tools

- Implement QC activities as necessary and monitor required quality metrics

Manage a cross functional project team ensuring all necessary project training is provided and developing a succession plan for the core team members. Manage projects in accordance with the contract including: study budget, study invoicing procedures, monitoring and reporting on progress of projects to stakeholders and implementing QC activities as necessary. Collaborate with business development to ensure proactive commercial aptitude while partnering with internal and external stakeholders to identify new avenues for growth. We do provide the flexible working type for this role. The major areas which prefers are the following:

With 2+ years' experience in full scope project management , at least 8 years' experience in pharmaceutical/clinical research industry; Thorough knowledge of ICH GCP and relevant regulations and a basic knowledge of the drug development and clinical trials process; Previous experience within the industry including a satisfactory progression of responsibility and relevant experience working within a project team within clinical, DM, Statistical management etc. The experience in leadership and/or management activities for a satisfactory progression is required; APAC Regional Project management experience is preferred; Excellent communication ability and skills for interacting among internal & external customer, especially in English; Diploma or above education background, major in clinical or pharmacy area is preferred.

The best candidate we anticipate is with fluent English Communication ability and with rich or plenty of experience in the cross-country management for the global trials for the various therapeutic areas.

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.

ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.

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