Project Manager
Talent Acquisition Team Lead
- Icon Strategic Solutions
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 drug and device development and commercialisation services to pharmaceutical, biotechnology, medical device and government and public health organisations. ICON Plc specialises in the strategic development, management and analysis of programs that support clinical development - from compound selection to Phase I-IV clinical studies. With headquarters in Dublin, Ireland, ICON employed approximately 15,250 employees in 94 locations in 40 countries as at September 30, 2020. Further information is available at www.iconplc.com.
Currently we are hiring the Project Managers in APAC Team
RWE Late Phase Research Services
Location : Korea (Office or home based)
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, 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 1+ 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 and Mandarin;
- Bachelor Science degree 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.
Comparing with our competitor and pharmaceutical companies, we provide more flexible and reasonable working platform for coach and educate the new comer to be a professional person to concentrate on relevant industry. ICON also provides the good package and benefit to adapt the marketing development.
We more like a whole family with kind-heart and warm carefulness which you can balance your life and work here.
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
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
Teaser label
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
Teaser label
Career ProgressionContent type
BlogsPublish date
11/26/2025
Summary
How Clinical Research Job Seekers Can Enhance Their Applications Finding the right role in clinical research has become increasingly competitive as organisations continue to expand their study por
Similar jobs at ICON
Salary
Location
Poland, Warsaw
Location
Warsaw
Remote Working
Office or Home
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate (CRA I and CRA II) to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and
Reference
JR139873
Expiry date
01/01/0001
Author
Zaklina LomberAuthor
Zaklina LomberSalary
Location
Canada, Burlington
Location
Burlington
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Medical Writing
Job Type
Permanent
Description
We are currently seeking a Senior Medical Writer to join our diverse and dynamic team. As a Senior Medical Writer at ICON, you will play a pivotal role in leading the development and execution of medi
Reference
JR140095
Expiry date
01/01/0001
Author
Brendan HoeyAuthor
Brendan HoeySalary
Location
US, Blue Bell (ICON)
Location
Multiple US Locations
Blue Bell
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Patient Recruitment
Job Type
Permanent
Description
We have an incredible opportunity for a Digital Media Buyer to join ICON’s Patient Recruitment Solutions (PRS) digital team. The Digital Media Buyer is responsible for digital advertising material and
Reference
JR136128
Expiry date
01/01/0001
Author
Tallulah PierreAuthor
Tallulah PierreSalary
Location
Canada, Montreal
Location
Montreal
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Permanent
Description
We are currently seeking a Study Start Up Associate I to join our diverse and dynamic team. As a Study Start Up Associate I at ICON, you will play a pivotal role in facilitating the initiation of clin
Reference
JR138612
Expiry date
01/01/0001
Author
Jasmine GarciaAuthor
Jasmine GarciaSalary
Location
US, Blue Bell (ICON)
Location
Burlington
Blue Bell
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Data Scientist Lead
Clinical Programming
Job Type
Permanent
Description
We are currently seeking a Clinical Data Validation Engineer to join our diverse and dynamic team. As a Senior Lead Clinical Data Science Programmer at ICON, you will be instrumental in leading the de
Reference
JR140098
Expiry date
01/01/0001
Author
Brendan HoeyAuthor
Brendan HoeySalary
Location
Colorado
Location
Colorado
California
Arizona
Utah
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
What You Will Be Doing:Serve as the primary point of contact between investigational sites and the sponsorConduct all types of site visits, including selection, initiation, routine monitoring, and clo
Reference
JR139958
Expiry date
01/01/0001
Author
Monica HawkinsAuthor
Monica Hawkins