Clinical Trial Manager
- UK
- ICON Strategic Solutions
- Clinical Trial Management
- Remote
About the role
This vacancy has now expired. Please see similar roles below...
We are hiring a Clinical Trial Manager working homebased in the UK to start on 06 May - this is mandatory requirement. Please only apply if you can meet this start date.
This is a great opportunity to steer your career towards clinical trial management. It would suit a Junior CTM, Senior CRA or experienced Senior Clinical Project Specialist with multiple country exposure, looking for their first CTM position.
You will be part of an innovative and global Biotechnology company, who pride themselves to be one of the world's leading independent biotechnology companies. They focus on areas with unmet medical need with the ambition to help reduce the social and economic burden of disease in society today.
The role
- Support the Global Clinical Trial Manager, Global Early Clinical Development Manager, Local Trial Manager, Regional or Country Study Manager in the delivery of the clinical and operational strategy and assist the execution of clinical trials
- Vendor management and support vendor relationships
- Work with the clinical trial management staff to support the execution and monitoring of clinical studies and trial deliverables
- Contribute to and support with the preparation, writing and review of study related documents including but not limited to, clinical protocols, study guides, monitoring plans, e(CRF)s, subject information sheets and consent forms, clinical study report, regulatory submissions and publications
- Coordinate the activities associated with site start-up and overall trial management
- Coordinate study level investigational product arrangements, accountability and reconciliation
- Contribute to, or coordinate preparation and conduct of site initiations, monitors’ workshops (as applicable) and investigator meetings (as applicable)
- Assists in preparing and managing Study Budgets and timelines
- Coordinate study level investigational product arrangements and study start-up and management activities
- Performprotocol-related site management activities
What is required
- BS/BA/BSc in the sciences preferred or RN or above
- 5 years’ work experience, ideally, in life sciences or medically related field, including 2 years of direct biopharmaceutical clinical research experience obtained working directly on clinical trials at a biotech, pharmaceutical or CRO company
- Project Management, project planning experience including oversight of study deliverables, study budgets, and timelines
- Experience interacting with external vendors (CROs, central labs, imaging vendors, etc.)
- Experience with development of prospective site – selection criteria
- Risk assessment, management and mitigation; delivery and risk focused
- Initiativeand critical thinking & planning ability
- Goodorganization, planning & communication skills
What is offered
- Solid structured on-boarding
- Full-time and permanent contract of employment with us seconded to one single sponsor
- Homebased in the UK/England
- Salary according to level of skills and experience
#LI-Remote:
#LI-EK1
Why Join?
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.
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, 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.
Application process
Once you find a job opening that fits your skills and interests, you can create an account, apply and check back on the progress of your application or apply for other roles. Once your application has been received, a confirmation email will be sent to your email.
Remember: this is our first time meeting you. Read the job description and highlight on your CV those experiences that we should learn about.
One of our experienced recruiters will read your profile and determine if you're fit for the role and the company. We are aware of instances where fake recruitment text messages and emails that can appear to come from ICON have been received by individuals. Always delete suspicious text messages or emails. Never give out personal financial information.
Reasonable AccomodationsDay in the life
Teaser label
Our PeopleContent type
BlogsPublish date
08/29/2023
Summary
To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her
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 stan
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 in-pe
Who we are
Similar jobs at ICON
Salary
Location
Argentina
Department
Clinical Trial Management
Location
Argentina
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Clinical Trial Manager 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
2023-103323
Expiry date
01/01/0001
Author
Tulio SanquizAuthor
Tulio SanquizSalary
Location
China, Beijing
Department
Clinical Trial Management
Location
Beijing
Chengdu
Guangzhou
Shanghai
Wuhan
Remote Working
Hybrid: Office/Remote
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
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 I
Reference
JR118474
Expiry date
01/01/0001
Author
Jessica ZhongAuthor
Jessica ZhongSalary
Location
China, Shanghai
Location
Beijing
Shanghai
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
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
Reference
JR118188
Expiry date
01/01/0001
Author
Jessica ZhongAuthor
Jessica ZhongSalary
Location
China, Beijing
Location
Beijing
Shanghai
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
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
Reference
JR118190
Expiry date
01/01/0001
Author
Jessica ZhongAuthor
Jessica ZhongSalary
Location
Belgium
Department
Clinical Trial Management
Location
Belgium
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
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
Reference
2024-109205
Expiry date
01/01/0001
Author
Tanzina GuerniAuthor
Tanzina GuerniSalary
Location
United Kingdom, Poland
Department
Clinical Trial Management
Location
Poland
UK
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Senior Clinical Scientist you will be supporting a global mid-sized biotech company. While being stably employed with ICON, you will be fully embedded with our client.
Reference
2024-108765
Expiry date
01/01/0001
Author
Natalia RothAuthor
Natalia Roth