Clinical Trial Manager
- Osaka, Tokyo
- ICON Full Service & Corporate Support
- Clinical Trial Management
- Office Based
About the role
This vacancy has now expired. Please click here to view live vacancies.
Clinical Trial Manager - Japan, Osaka
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Senior Centralized Clinical Trial Manager to join our diverse and dynamic team. As a Senior Centralized Clinical Trial Manager at ICON, you will play a pivotal role in overseeing and optimizing centralized clinical trial operations, ensuring the efficient and effective execution of trials to contribute to the advancement of innovative treatments and therapies.
What You Will Be Doing:- Develop and implement comprehensive operational strategies to streamline centralized clinical trial processes and ensure compliance with regulatory requirements.
- Lead a team of clinical trial specialists, providing guidance and support to ensure adherence to protocols and regulatory standards.
- Collaborate with cross-functional teams, including project managers, data managers, and clinical monitors, to facilitate seamless coordination and communication.
- Analyze centralized trial processes and protocols, identifying areas for improvement and implementing enhancements to increase efficiency and accuracy.
- Monitor and report on key performance indicators (KPIs) to ensure that trial goals and targets are met.
- Bachelor's degree in a relevant field, such as Life Sciences, Medicine, or a related discipline; advanced degree preferred.
- Proven experience in a leadership role within the clinical research or pharmaceutical industry, with a strong understanding of centralized clinical trial processes and regulatory requirements.
- Excellent analytical and problem-solving skills, with the ability to identify and address operational inefficiencies.
- Strong project management skills, with the ability to prioritize tasks, manage multiple projects simultaneously, and meet deadlines.
- Exceptional communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external stakeholders.
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
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, colour, 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 or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
Explore more about ICON
Day in the life
Teaser label
Career ProgressionContent type
BlogsPublish date
02/17/2023
Summary
Clinical Trial Managers and Clinical Project Managers are an integral part of the clinical market. Each role is essential in ensuring that clinical trials are well run and completed to a high
Teaser label
Inside ICONContent type
BlogsPublish date
10/03/2022
Summary
In traditional clinical trials, patients must attend regular check-ins at hospitals or clinics but fully remote decentralised clinical trials (DCTs) and hybrid trials limit this by replacing the
Teaser label
Career ProgressionContent type
BlogsPublish date
07/06/2022
Summary
It's not hard to reel off a list of reasons to become a Medical Director. The chance to ensure that patient care is high-quality will likely be right at the top. But why should you bring your M
Similar jobs at ICON
Salary
Location
United States of America
Location
Multiple US Locations
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programs.What You
Reference
JR151489
Expiry date
01/01/0001
Author
Jonathan HolmesAuthor
Jonathan HolmesSalary
Location
US, Blue Bell (ICON)
Department
Clinical Trial Management
Location
Blue Bell
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.
Reference
JR156112
Expiry date
01/01/0001
Author
Michael HartleyAuthor
Michael HartleySalary
Location
UK, Reading
Location
Reading
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.What Yo
Reference
JR155148
Expiry date
01/01/0001
Author
Rajvir SamraAuthor
Rajvir SamraSalary
Location
Hungary, Budapest
Location
Budapest
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.What Yo
Reference
JR155715
Expiry date
01/01/0001
Author
Orsolya BerkeAuthor
Orsolya BerkeSalary
Location
Spain, Madrid
Department
Clinical Trial Management
Location
Sofia
Prague
Budapest
Vilnius
Warsaw
Lisbon
Bucharest
Barcelona
Madrid
Bratislava
Tbilisi
Gdansk
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.What Yo
Reference
JR155967
Expiry date
01/01/0001
Author
Katty Barreto MaiaAuthor
Katty Barreto MaiaSalary
Location
Brazil, Sao Paulo
Location
Sao Paulo
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
Our Real World Solutions Team is looking for an experienced Clinical Trial Manager (CTM) that will be responsible for the end-to-end operational oversight of assigned clinical trials, ensuring deliver
Reference
JR154501
Expiry date
01/01/0001
Author
Ana LuciaAuthor
Ana Lucia