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Full Service Clinical Operations

We have multiple opportunities in Clinical Operations across our full service divisions- ICON Pharma Solutions & ICON Biotech Solutions.

Learn more about this division, or skip straight to our latest Clinical Operations jobs.


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ICON Pharma Solutions careers in Clinical Operations

Clinical Operations and Research specialists at ICON apply therapeutic, regulatory and operational expertise to solve challenges that may arise during a clinical project.

We have a wide variety of opportunities within clinical operations, development and research and there are many divisions that we recruit for. This includes development programme management, site and clinical trial management, clinical trial monitoring, patient recruitment, contract management and investigator reimbursement, and we have vacancies available across the globe.

We’re proud to have the experience and knowledge to find and keep patients for our client trials in the face of an increasingly challenging environment. Our comprehensive expertise in scientific and operational areas by our Lifecycle Sciences group offers the finest strategic consultancy available within the industry.

ICON Biotech Solutions careers in Clinical Operations

Our Biotech Clinical Delivery team is unique. We have built Clinical Delivery as an all-inclusive function: Clinical Team Managers, Clinical Research Associates and Site Feasability Specialists work side by side. If you are looking for that ‘small team’ feeling, you have found it!

Our goals include strategically evaluating study needs, prioritising deliverables and exceeding client expectations. You’ll have the support of the best-in-industry leadership, with boundless options for career growth within our unit and across ICON.

Come join our growing team! We have openings across the Globe.

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Clinical Monitoring - ICON Pharma Solutions & ICON Biotech Solutions

As a Pharma Solutions CRA, you have the opportunity to work in a variety of different protocols and Therapeutic Areas you are not aligned with, which gives you so much more opportunity to keep learning. We also run indication-specific internal ‘Universities’ to provide that extra layer of knowledge if someone hasn’t been exposed to a certain area before. Our Management team in the clinical operations group has been a part of the ICON for a long time and can support you with the growth of your career – we are also very proud to say that many of them have joined us as CRAs and are home-grown. We offer thousands of practical and diverse training modules available through our in-house training programme. With a mixture of instructor-led, self-learning or in-person classroom settings.

As a Biotech Solutions CRA, you will have the ability to develop a broad therapeutic experience. CRAs may have the opportunity to work on Phase I studies, niche treatments, blockbuster drugs or biosimilars. Our Biotech CRAs will work on a minimal number of protocols and sponsors and have dedicated functional managers who are not assigned to billable work. ICON offers a wide range of CRA perks.

Study Start Up - ICON Pharma Solutions & ICON Biotech Solutions

The ICON Pharma Solutions Study Start-Up (SSU) group covers Feasibility, Site Identification, and Start-Up. Having all these services under one roof provides the ability to remain focused on delivering the best sites faster than our competitors. We are proud of our industry-beating cycle times! Our award-winning study execution capabilities have led to the approval of 18 of the world’s top 20 best-selling drugs. As a member of the Study Start-Up Team, you will play an integral role in making sure that physicians at our research sites are prepared to start the trial of investigational, new pharmaceutical and biological products for clinical trials at their local practices.

Our goal is to directly impact patients' lives by expediting access to our clients' innovations during the initial stages of clinical trials. We offer our clients best practices, critical path-focused cycle times, and a consistent global approach to activate sites with urgency. There are 4 main service lines – Management, Delivery, Contracts, and Site Partnerships – coming together as one team, each playing a key part in leading our trials from start up to the implementation of our client’s trials.

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Clinical Trial Management - ICON Pharma Solutions & ICON Biotech Solutions

In ICON Pharma Solutions, our Clinical Trial Managers are responsible for the delivery of all clinical aspects of the study. Overseeing the clinical portion of the budget, developing monitoring plans & tools, training CRAs, driving enrolment and study start-up activities. There are multiple opportunities for training and career growth as well as opportunities to mentor and participate in company initiatives.

Our Biotech Solutions Clinical Trial Managers work in a collaborative work environment with user-friendly dashboards to help identify and mitigate risk. We have a customer and therapeutic-focused delivery team across roles that allow for enhanced communication and effectiveness. There are multiple opportunities for training and career growth as well as opportunities to mentor and participate in company initiatives.

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Mariagabriela Alterio
Vice President, ICON Pharma          Clinical Operations Latin America

List #1

Roles in this area at ICON

CRA II/Senior CRA

Salary

Location

Poland, Warsaw

Department

Clinical Monitoring

Location

Warsaw

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

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

Reference

JR138386

Expiry date

01/01/0001

Tereza Svobodova Read more Shortlist Save this role
CSA

Salary

Location

France, Paris

Department

Clinical Monitoring

Location

Paris

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

Clinical Site Associate (CSA) We are currently seeking a Clinical Site Associate (CSA) to join our diverse and dynamic team. As an CSA at ICON, you will play a pivotal role in supporting clinical tria

Reference

JR132369

Expiry date

01/01/0001

Sophie Clarke

Author

Sophie Clarke
Read more Shortlist Save this role
Senior TMF Specialist

Salary

Location

India, Chennai

Department

Clinical Trial Management

Location

Bangalore

Chennai

Bengaluru

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Regulatory Document Management

Job Type

Permanent

Description

Location: Chennai (Hybrid)What are we looking for:Should have 4-5 years Data Analytics IT experience.Should be specialized in Data Cleaning, Transformation, ModellingShould have experience in dashboar

Reference

JR135817

Expiry date

01/01/0001

Moushami Roy

Author

Moushami Roy
Read more Shortlist Save this role
CRA II/ Senior CRA

Salary

Location

Germany, Frankfurt

Department

Clinical Monitoring

Location

Frankfurt

Remote Working

Office or Home

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

JR138301

Expiry date

01/01/0001

Jakob Schonberger Read more Shortlist Save this role
In-House Clinical Research Associate

Salary

Location

Turkey, Ankara

Department

Clinical Monitoring

Location

Ankara

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

We are currently seeking an In-House Clinical Research Associate to join our diverse and dynamic team. As an IHCRA at ICON, you will play a pivotal role in supporting the execution and management of c

Reference

JR130319

Expiry date

01/01/0001

Jacek Jaworski Read more Shortlist Save this role
Clinical Site Associate (CSA)

Salary

Location

Hungary, Budapest

Department

Clinical Monitoring

Location

Budapest

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

Clinical Site Associate (CSA) We are currently seeking a Clinical Site Associate (CSA) to join our diverse and dynamic team. As an CSA at ICON, you will play a pivotal role in supporting clinical tria

Reference

JR138141

Expiry date

01/01/0001

Teodora  Kaykieva Read more Shortlist Save this role
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