Clinical Research Jobs in United Kingdom

Search and find our latest clinical research jobs based in the United Kingdom. We have jobs available in London and all over the UK, for more information contact us or apply directly to our jobs below.

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As a Principal Biostatistician you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

2023-104906

Expiry date

UK, Reading

Clinical Monitoring

Real World Solutions

Hybrid: Office/Remote

ICON Full Service & Corporate Support

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, biotech

Tereza Svobodova

Johannesburg

Data Standards Consultant

Sophia Cairns

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

2024-109014

Amani Yousef

Clinical Operations Roles

Clinical Trial Support

2024-108519

United Kingdom

Clinical Trial Management

We are hiring 2 Project Managers with global clinical studies experience to start  begininng of May (this is mandatory!). You will work fully UK home-based  Do you have experience of managing internat

2024-108991

Regional Scotland (PRA)

Office Based

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

Nandhini Selvakumar

UK-Based experienced In Vitro Diagnostics CRA required to augment existing team of IVD CRAs. Target candidate profiles are >BSc educated UK-based experienced CRAs with a Lab-based background. You will

2024-109281

United Kingdom, Germany, France, Spain, Poland

Clinical Data Management

Clinical Data Scientist Lead

Clinical Systems

2024-109450

UK homebased Clinical Trial Manager performing Clinical Risk Manager (CRM) dutiesAre you an experienced Clinical Research or Clinical Project Manager with a flair for innovation, team leadership and e

2024-109448

UK, Northhamptonshire (Accellacare)

Northhamptonshire

Temporary Employee

Site AdministratorOffice-based - CorbySix-month fixed-term contractICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinica

Hajni Howard

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An Evolution of Progress and Success: Zashan's story a Clinical Research Associate (CRA) Having a satisfying career involves finding a company that prioritizes progress, improvement, and chances f

Zashan, who began his journey with us in 2016, has shared his experience and insights.

  • Employee Stories -

A picture of Debora Oh

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

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

contract clinical research associate jobs uk

ICON plc's Global CRA Academy Program and the Argentina Success Story In the ever-evolving realm of clinical research, the role of Clinical Research Associates (CRAs) continues to be in a critica

While ICON's CRA Academy program is a global initiative, our focus is on the success story that has unfolded in Argentina.

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contract clinical research associate jobs uk

Senior Clinical Research Associate (CRA) - UK - Home-based

Worldwide Clinical Trials

Job Details

  • Conduct all types of visits - site qualifications, initiation, interim monitoring, site management and study close-out visits
  • Review study subject safety information and informed consent and conduct source document verification for compliance, patient safety, and veracity of data
  • Actively participate in study team and investigator meetings
  • Compile and ensure completeness of regulatory documents and ethical submission documentation and review study subject safety information and informed consent and study material (e.g. CRFs, manuals)
  • Excellent interpersonal, oral, and written communication skills in English and local language
  • Superior organizational skills with attention to details, and the ability to work independently
  • Broad understanding of clinical research principles and process
  • Proficiency in Microsoft Office, CTMS and EDC Systems
  • At least two years independent clinical monitoring experience
  • Demonstrable experience of handling multiple protocols across a range of therapeutic indications
  • Four-year college curriculum in life sciences, OR Two-year college curriculum or equivalent education / training (nursing degree or equivalent life science degree)
  • Ability to meet the travel requirements of the job

Find out more about working for our company

Worldwide Clinical Trials -hub-button

Brief Company Description; 

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,000 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

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