JUMP TO CONTENT
Shortlist
search jobs Search
About the role ICON and you Application Process Day in the life Who we are

CTA

042704_2

About the role

This vacancy has now expired. Please see similar roles below...

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our Clinical Trial Assistants (CTA’s) play a key role within ICON.  Working closely with our global clinical teams the Clinical Trial and Project Managers to ensure the efficient and effective conduct of clinical trial studies. 
 
Overview of the role
  • You will need to ensure high levels of accuracy when completing tasks, you will set up, manage and maintain clinical study documentation and coordinate the ordering, dispatch and tracking of study materials.  You will support the project teams by updating the Clinical Trial Management Systems. 
  • You will arrange and attend internal and external meetings, helping to produce presentation materials and generate meeting minutes. You will also assist in the tracking and distribution of safety reports and coordinate document translations if required.   
  • Contacting external and internal individuals; you will collate relevant study information and assist with study payments.  You should be prepared to take on any additional tasks assigned as and when required. 
Role Requirements  
  • You will possess sufficient administrative experience within a busy environment where you have demonstrated excellent organisation and prioritization skills or hold a bachelor’s degree in a science related field.   Your experience of prioritising a demanding workload and ability to produce work to tight deadlines will be essential for this role. 
  • You must possess previous working knowledge of Word, Excel, Outlook and PowerPoint. 
  • You will be fluent in English and the local language for the country you are applying. You will have excellent communication skills, both written and verbal, enabling you to deal with queries in a timely manner.  A confident team player, your interpersonal experience will be the key to developing and maintaining relationships both internally and externally.  
Benefits of Working in ICON
 
Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package.  This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
 
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.   
 
What’s Next?
 
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.
 
ICON is an equal opportunity employer -  M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
List #1

Day in the life

Medics in a room talking
Communication Strategies for Sites and Sponsors

Teaser label

Industry

Content type

Blogs

Publish date

12/16/2024

Summary

Effective Communication with Sites and Sponsors in Clinical Research Clear and effective communication is the cornerstone of successful clinical research. It fosters collaboration, ensures complia

Teaser label

Discover effective communication strategies for clinical research sites and sponsors.

Read more
Person writing with a pen on a clipboard
What Is Medical Writing? A Comprehensive Guide for Beginners

Teaser label

Industry

Content type

Blogs

Publish date

12/16/2024

Summary

Medical Writing - A Comprehensive Guide for Beginners Medical writing is a specialized field that bridges science and communication. It plays a critical role in the healthcare, pharmaceutical, and

Teaser label

Explore the world of medical writing in this comprehensive guide.

Read more
Image of phone, laptop, and monitor
Comprehensive Guide to Electronic Data Capture (EDC) Systems

Teaser label

Industry

Content type

Blogs

Publish date

12/11/2024

Summary

Electronic Data Capture (EDC) Systems In the rapidly evolving landscape of clinical research, Electronic Data Capture (EDC) systems have emerged as indispensable tools, transforming the way clinica

Teaser label

Discover how Electronic Data Capture (EDC) systems are revolutionising clinical trials.

Read more
View all

Similar jobs at ICON

Senior Statistical Programmer II

Salary

Location

China, Beijing

Location

Beijing

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Programming

Job Type

Permanent

Description

We are currently seeking a Senior Statistical Programmer II to join our diverse and dynamic team. As a Senior Statistical Programmer II at ICON, you will play a vital role in the analysis and reportin

Reference

JR126308

Expiry date

01/01/0001

Jessica Zhong

Author

Jessica Zhong
Jessica Zhong

Author

Jessica Zhong
Read more Shortlist Save this role
Read more Shortlist Save this role
CRA II

Salary

Location

Netherlands

Department

Clinical Monitoring

Location

Netherlands

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

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

2024-115831

Expiry date

01/01/0001

Iris Brouwer

Author

Iris Brouwer
Iris Brouwer

Author

Iris Brouwer
Read more Shortlist Save this role
Read more Shortlist Save this role
Data Analyst I - Radiography, CT & MRI exp.

Salary

Location

India, Chennai

Department

Full Service - Development & Commercialisation Solutions

Location

Chennai

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Data Management

Analyst

Job Type

Permanent

Description

The RoleResponsibilities include data analysis, quality assurance, and data formatting according to specifications that are either predefined, or as determined based on analysis of business need. Orig

Reference

JR126949

Expiry date

01/01/0001

Puja Jaiswal

Author

Puja Jaiswal
Puja Jaiswal

Author

Puja Jaiswal
Read more Shortlist Save this role
Read more Shortlist Save this role
Payroll Associate

Salary

Location

India, Chennai

Location

Chennai

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Human Resources

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

JR124339

Expiry date

01/01/0001

Monisha MJ

Author

Monisha MJ
Monisha MJ

Author

Monisha MJ
Read more Shortlist Save this role
Read more Shortlist Save this role
Principal Medical Writer

Salary

Location

Belgium, United Kingdom, Denmark, France, Spain, Germany, Netherlands, Switzerland

Department

Medical Affiars & Medical Writing Roles

Location

Belgium

Denmark

France

Germany

Netherlands

Spain

Switzerland

UK

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Medical Writing

Job Type

Permanent

Description

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

Reference

2023-103952

Expiry date

01/01/0001

Natalia Roth

Author

Natalia Roth
Natalia Roth

Author

Natalia Roth
Read more Shortlist Save this role
Read more Shortlist Save this role
Global Regulatory Lead - United States, Part Time

Salary

Location

United States

Department

Regulatory, Drug Safety/ Quality Assurance & Other roles

Location

United States

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Regulatory Affairs

Job Type

Permanent

Description

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

Reference

2024-115379

Expiry date

01/01/0001

Read more Shortlist Save this role
Read more Shortlist Save this role

Browse popular job categories below or search all jobs above