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

Clinical Trial Manager

014098_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. This role sits within our Late Phase team (IIIb/IV) where our Clinical Trial Managers act as the Functional Lead with responsibility for delivery of all Clinical Operations aspects of late phase studies.
 
Overview of the role
  • As a Manager, you would be expected to recognize the importance of and create a culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
  • Primary point of contact for Clinical Operations aspects of designated projects and responsible for developing successful working relationships with clients
  • Responsible for planning, scheduling and implementing the Clinical Operations aspects of projects
  • Contribute to the development and maintenance of cross functional project management plans
  • Responsible for risk mitigation strategies, associated action plan and issue resolution
  • Responsible for managing the Clinical Operations project team, including ensuring all necessary project training is provided to assigned staff
  • Provide direction and support to the Clinical Operations study team
  • Collaborate with Business Development (BD) to ensure timely completion of change orders
  • Track Clinical Operations project deliverables using appropriate tools 
Role Requirements  
  • University/Bachelor’s Degree in medicine, science or equivalent degree/experience.
  • A satisfactory progression of monitoring experience with previous experience in leadership and/or management activities
  • Previous working experience within the Late Phase (IIIb/IV) clinical trial management field.
  • Thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials.
  • Some knowledge of project management processes and tools.
  • Fluent in written and spoken English. 
  • Computer literate.
  •  Due to the nature of this position it may be required for the employee to travel approx 25%.  Therefore, dependent on the employee’s location, the employee may be required to possess a valid Driver’s license  
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, if successful, you will be contacted by one of our dedicated recruiters who 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

3 x Digital padlocks
The Role of Cybersecurity in Clinical Data Management

Teaser label

Industry

Content type

Blogs

Publish date

07/04/2025

Summary

Cybersecurity in Clinical Data Management In clinical research, data is both a vital asset and a significant responsibility. As trials become increasingly digitised and decentralised, the protectio

Teaser label

Learn about the critical role cybersecurity plays in an increasingly digital research environment.

Read more
Stethoscope on paper
Specialisations in Clinical Research: Finding Your Niche

Teaser label

Industry

Content type

Blogs

Publish date

07/03/2025

Summary

Finding the Specialisation for You Clinical research is a dynamic, multidisciplinary field that brings together scientific innovation, operational rigour and patient-centric thinking. While many

Teaser label

Explore the diverse specialisations in clinical research, from clinical operations to data management, regulatory affairs, and beyond.

Read more
People talking in a meeting
Networking Strategies in Clinical Research

Teaser label

Industry

Content type

Blogs

Publish date

06/06/2025

Summary

Building Connections that Drive Progress In an industry where collaboration is critical to advancing science and improving patient outcomes, networking is more than a professional courtesy - it’s

Teaser label

Discover how strategic networking can strengthen collaboration, and support your clinical research career journey.

Read more
View all

Similar jobs at ICON

Senior Site Contracts Lead

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Remote Working

Home or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Study Start Up

Job Type

Permanent

Description

Senior Site Contracts LeadResponsible for overall oversight, management, and delivery of site contracts for assigned studies at country, regional, or global level and other site contracting projects a

Reference

JR128419

Expiry date

01/01/0001

Daniela Guerrero

Author

Daniela Guerrero
Daniela Guerrero

Author

Daniela Guerrero
Read more Shortlist Save this role
Read more Shortlist Save this role
Site Contracts Lead

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Remote Working

Home or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Contracts Administration

Job Type

Permanent

Description

Title: Site Contracts LeadResponsible for overall oversight, management, and delivery of site contracts for assigned studies at country, regional, or global level.Responsibilities:In collaboration wit

Reference

JR128195

Expiry date

01/01/0001

Daniela Guerrero

Author

Daniela Guerrero
Daniela Guerrero

Author

Daniela Guerrero
Read more Shortlist Save this role
Read more Shortlist Save this role
CTA

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and a

Reference

JR126281

Expiry date

01/01/0001

Read more Shortlist Save this role
Read more Shortlist Save this role
Senior CRA

Salary

Location

Santiago

Department

Clinical Monitoring

Location

Santiago

Remote Working

Office Based

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will be partnering with one of our

Reference

2025-120592

Expiry date

01/01/0001

Magda Obregon

Author

Magda Obregon
Magda Obregon

Author

Magda Obregon
Read more Shortlist Save this role
Read more Shortlist Save this role
Senior CRA

Salary

Location

Santiago

Department

Clinical Monitoring

Location

Santiago

Remote Working

Office Based

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will be partnering with one of our

Reference

2025-120593

Expiry date

01/01/0001

Magda Obregon

Author

Magda Obregon
Magda Obregon

Author

Magda Obregon
Read more Shortlist Save this role
Read more Shortlist Save this role
Program Manager, FSA

Salary

Location

Poland, Warsaw

Location

Sofia

Prague

Dublin

Riga

Warsaw

Lisbon

Belgrade

Bratislava

Remote Working

Home or Office

Business Area

ICON Full Service & Corporate Support

Job Categories

Study Start Up

Job Type

Permanent

Description

Application Deadline: 11th July 2025 Accountable for driving and accelerating the activation of global investigative sites in line with, or ahead of, the study's contractual timelines, within budgeted

Reference

JR132104

Expiry date

01/01/0001

Magda Kozuszek

Author

Magda Kozuszek
Magda Kozuszek

Author

Magda Kozuszek
Read more Shortlist Save this role
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above