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Clinical Trial Manager - local

  1. Reading
JR121093
  1. ICON Full Service & Corporate Support
  2. Clinical Trial Management
  3. Hybrid: Office/Remote

About the role

About the role

Clinical Trial Manager - Sponsor Dedicated

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.

About the role:

The Clinical Trial Manager is responsible for the delivery of all clinical aspects of the study within the UK for one of our sponsors - a global pharmaceutical.


The CTM oversees the clinical portion of the budget, develops monitoring plans & tools, trains CRAs, drives enrolment and study start-up activities, reviews trip reports, implements corrective and preventative action plans, liaises with the Sponsor, vendors & cross-functional teams, identifies & mitigates risks that may impact clinical delivery, and provides reporting & metrics on all clinical activities.
The CTM will also participate in Sponsor, Investigator and bid defense meetings.

You will need:
• Lifesciences/Science degree or equivalent combination of education & experience
• Demonstrated ability to drive the clinical deliverables of a study as a Clinical Trial Lead/Manager, including submissions experience- essential
• Prior monitoring experience as a Senior CRA is preferred
• Ability to travel up to 20%


Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON 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.

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Day in the life

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How to excel as a CRA in a Clinical Research Organisation

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Our People

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Publish date

08/29/2023

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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

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Brazil-based CRA II Debora Oh shares her tips on how to become a great CRA and provides insight into life at ICON.

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What is the difference between a clinical trial manager and a clinical project manager?

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Career Progression

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Publish date

02/17/2023

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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

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Are remote decentralised clinical trials the future?

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10/03/2022

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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

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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

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