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

Clinical Research Associate

012653_2

About the role

This vacancy has now expired. Please click here to view live vacancies.
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. Working within a highly qualified team our Clinical Research Associates (CRA's) identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV ensuring adherence to applicable regulations and principles of ICH-GCP.
 
Overview of the Role
  • Working independently and proactively to coordinate all necessary activities required for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation.  You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested. 
  • Managing sponsor generated queries efficiently and taking responsibility for study cost effectiveness; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.  
  • Depending on your level of experience, you may assist in training and mentoring less experienced CRA's and/or manage CRA's working on international projects. 
Role Requirements  
  • With a University degree in medicine, science, or equivalent; you will have previous monitoring experience in medium sized studies, including study start-up and close-out (for all roles above Entry Level).  You should also have knowledge of ICG GCP guidelines and the expertise to review and evaluate medical data.   
  • Fluent in English, as well as the local language, you will possess excellent written and verbal communication and interpersonal skills enabling you to deal with queries in a timely manner.  You should be able to produce accurate work to tight deadlines within a pressurised environment. 
  • You must be available to travel at least 60% of the time (international and domestic -fly and drive) and should possess a valid driving licence. 
  • You will have the opportunity to progress your career and may wish to move into Project Management or into other related areas where you can further develop your skill set.  
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

Liquid drug vials in palm of hand
Understanding INDs and NDAs in Clinical Research

Teaser label

Industry

Content type

Blogs

Publish date

04/22/2025

Summary

What is an IND or NDA? A Guide for Aspiring Clinical Research Professionals If you’re considering a career in clinical research or the broader pharmaceutical and biotech industry, you’ve likely c

Teaser label

Discover the difference between IND & NDA applications, and the steps from drug development to regulatory approval.

Read more
Informed consent form
What is an Informed Consent Form (ICF)?

Teaser label

Industry

Content type

Blogs

Publish date

04/22/2025

Summary

When it comes to clinical trials, one of the most important documents you’ll hear about is the Informed Consent Form (ICF). Whether you're starting out in clinical research or exploring job opportunit

Teaser label

Learn what an Informed Consent Form (ICF) is, why it’s essential in clinical research, and how it protects participants.

Read more
Medic in full gown with a clipboard
Clinical Research Associate (CRA) vs Clinical Research Coordinator (CRC)

Teaser label

Industry

Content type

Blogs

Publish date

04/17/2025

Summary

CRA vs CRC Embarking on a career in clinical research is an exciting journey for STEM graduates, offering opportunities to contribute directly to the development of new therapies and to safeguard

Teaser label

Discover the key differences between Clinical Research Associates (CRA) and Clinical Research Coordinators (CRC).

Read more
View all

Similar jobs at ICON

Senior Drug Development Project Manager - Home-Based (East Coast)

Salary

Location

United States

Department

Project Management Roles

Location

United States

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Project Management

Job Type

Permanent

Description

The Drug Development Project Manager (Senior Drug Development Director) oversees the high-level plans and progress of these teams, managing projects from pre-clinical stages through to commercializati

Reference

2025-119093

Expiry date

01/01/0001

Kala Murphy

Author

Kala Murphy
Kala Murphy

Author

Kala Murphy
Read more Shortlist Save this role
Read more Shortlist Save this role
Senior Drug Development Project Manager - Home-Based (East Coast)

Salary

Location

United States

Department

Project Management Roles

Location

United States

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Project Management

Job Type

Permanent

Description

The Drug Development Project Manager (Senior Drug Development Director) oversees the high-level plans and progress of these teams, managing projects from pre-clinical stages through to commercializati

Reference

2025-119094

Expiry date

01/01/0001

Kala Murphy

Author

Kala Murphy
Kala Murphy

Author

Kala Murphy
Read more Shortlist Save this role
Read more Shortlist Save this role
In Vivo Toxicologist

Salary

Location

Reading

Department

Medical Affiars & Medical Writing Roles

Location

Reading

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Medical & Scientific Affairs

Job Type

Permanent

Description

UK-based In Vivo Toxicologist. Home based, United Kingdom (12 month contract).  You will be partnering with a well-known global pharmaceutical company with a strong portfolio in cardiovascular, gastro

Reference

2025-119100

Expiry date

01/01/0001

Dominic Brady

Author

Dominic Brady
Dominic Brady

Author

Dominic Brady
Read more Shortlist Save this role
Read more Shortlist Save this role
SSUA II/ Senior SSUA

Salary

Location

Turkey, Ankara

Location

Ankara

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Study Start Up

Job Type

Permanent

Description

We are currently seeking a Study Start Up Associate II to join our diverse and dynamic team. As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinica

Reference

JR129137

Expiry date

01/01/0001

Katty Barreto Maia

Author

Katty Barreto Maia
Katty Barreto Maia

Author

Katty Barreto Maia
Read more Shortlist Save this role
Read more Shortlist Save this role
CRA II

Salary

Location

Czech Republic, Prague

Department

Clinical Monitoring

Location

Prague

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Clinical Research Associate II Specialist to join our diverse and dynamic team. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal role in desig

Reference

JR129828

Expiry date

01/01/0001

Tereza Svobodova

Author

Tereza Svobodova
Tereza Svobodova

Author

Tereza Svobodova
Read more Shortlist Save this role
Read more Shortlist Save this role
Contract Analyst

Salary

Location

Turkey, Ankara

Location

Ankara

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Corporate Support

Job Type

Permanent

Description

We are currently seeking a Contract Analyst to join our diverse and dynamic team. As a Contract Analyst at ICON, you will play a pivotal role in facilitating the initiation of clinical trials, ensurin

Reference

JR129118

Expiry date

01/01/0001

Katty Barreto Maia

Author

Katty Barreto Maia
Katty Barreto Maia

Author

Katty Barreto Maia
Read more Shortlist Save this role
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above