Senior Clinical Trial Manager
Talent Acquisition Team Lead
- Icon Strategic Solutions
About the role
This vacancy has now expired. Please click here to view live vacancies.
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
Senior Clinical Trial Manager
Taiwan
JOB FUNCTIONS/RESPONSIBILITIES
- Primary point of contact for Clinical Operations aspects of designated projects and responsible for developing successful working relationships with clients
- Responsible for planning, scheduling and implementing the Clinical Operations aspects of projects
- Contribute to the development and maintenance of cross functional project management plans
- Responsible for risk mitigation strategies, associated action plans and issue resolution
- Responsible for managing the Clinical Operations project team, including ensuring all necessary project training is provided to assigned staff
- Provide direction and support to the Clinical Operations study team
- Manage Clinical Operations aspects of projects in accordance with the contract including communicate any changes in Clinical Operations scope to the Project Manager and collaborate with Business Development to ensure timely completion of change orders
- Track Clinical Operations project deliverables using appropriate tools
- Effectively monitor and report on progress of the Clinical Operations aspects of projects to all stakeholders
- Implement QC activities as necessary and monitor required quality metrics
- Participate in business development activities, as appropriate including bid defense and proposal activities
- Responsible for managing the Clinical Operations project team, including ensuring all necessary project training is provided to assigned staff
EXPERIENCE, SKILLS, KNOWLEDGE REQUIREMENTS
- Experience in Clinical Trial Management roles or equivalent role and 7+ years of total experience in the clinical research field.
- Successful industry experience, of clinical trial management and a proven understanding of the clinical operations aspects of projects and how they impact/interact with other functions
- Thorough knowledge of ICH GCP and relevant regulations and a basic knowledge of the drug development and clinical trials process.
- Proven leadership and ability to make complex decisions with minimum management oversight and work independently within the role
- Knowledge of Clinical Operations processes and tools
- University/Bachelor's Degree, or local equivalent, in medicine, science or equivalent degree/ experience
- Fluent in written and spoken English and Chinese
- Computer literate.
- Due to the nature of this position it may be required for the employee to travel both domestically and internationally.
Benefits of Working in ICON
Our success depends on the knowledge, capabilities and quality of our people. That's why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
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. See all locations Learn more about Our Culture at ICON
Day in the life
.png)
Teaser label
IndustryContent type
BlogsPublish date
07/07/2025
Summary
Precision at the Outset: The Strategic Role of Site Selection and Activation in Clinical Trials The success of any clinical trial begins well before the first patient is enrolled. Behind every sit
.png)
Teaser label
IndustryContent type
BlogsPublish date
07/04/2025
Summary
Cybersecurity in Clinical Data Management In clinical research, data is both a vital asset and a significant responsibility. As trials become increasingly digitised and decentralised, the protectio
.png)
Teaser label
IndustryContent type
BlogsPublish date
07/03/2025
Summary
Finding the Specialisation for You Clinical research is a dynamic, multidisciplinary field that brings together scientific innovation, operational rigour and patient-centric thinking. While many
Similar jobs at ICON
Salary
Location
Orlando
Department
Clinical Monitoring
Location
Orlando
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-120774
Expiry date
01/01/0001
Author
Monica HawkinsAuthor
Monica HawkinsSalary
Location
US, Lenexa KCIB (PRA)
Department
Full Service - Early Clinical and Bioanalytical Solutions
Location
Lenexa
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Pharmacy
Job Type
Permanent
Description
Job Title: Research Pharmacy TechnicianJob Location: On-site - Lenexa, KSJob Type: Full-TimeWe are currently seeking a Research Pharmacy Technician to join our diverse and dynamic team. As a Research
Reference
JR132109
Expiry date
01/01/0001
Author
Michael HartleyAuthor
Michael HartleySalary
Location
Argentina
Department
Clinical Operations Roles
Location
Argentina
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a Site Management Associate I (SMA I) you will have the opportunity to work with one of the world’ s leading pharma & biotech companies, helping them advance new drugs and devices. You will play a
Reference
2025-120630
Expiry date
01/01/0001
Author
Tulio SanquizAuthor
Tulio SanquizSalary
Location
Argentina
Department
Biometrics Roles
Location
Argentina
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Data Management
Clinical Data Scientist Lead
Clinical Systems
Data Standards Consultant
Job Type
Permanent
Description
(Talent pool) As a Clinical Data Coordinator you will play a key role in improving the lives of patients by accelerating the development of our customers drugs and devices through innovative solutions
Reference
2025-116863
Expiry date
01/01/0001
Author
Tulio SanquizAuthor
Tulio SanquizSalary
Location
Brazil
Department
Clinical Operations Roles
Location
Brazil
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a CTA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-120646
Expiry date
01/01/0001
Author
Bruna DuarteAuthor
Bruna DuarteSalary
Location
Portugal
Department
Clinical Monitoring
Location
Portugal
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Clinical Research Associate (CRA) you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations and standard o
Reference
2025-120777
Expiry date
01/01/0001
Author
Lola PomboAuthor
Lola Pombo