JUMP TO CONTENT

Application Analyst I

010928_2

About the role

This vacancy has now expired. Please click here to view live vacancies.

DEPARTMENT: Clinical Operations

JOB TITLE: Application Analyst I

REPORTS TO: Associate Director, System Administration and Support Project Technology Support or Designee

 

SECTION 1: POSITION SUMMARY

 

• Provide system administration and support for assigned applications.
• Provide support for application development projects.

 

SECTION 2: JOB FUNCTIONS/RESPONSIBILITIES

 

• Recognize, exemplify and adhere to ICON's values which centers around our commitment to People, Clients and Performance.
• As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
• Travel (approximately 0%) domestic and/or international
• Provide timely, high quality support for system users.
• Interface with users to collect study set up requirements.
• Complete technical set-up of studies.
• Interface with IT to evaluate, resolve and communicate system-related issues impacting users and escalate to Application Manager and Support Manager as applicable.
• Escalate application issues with a perceived high user impact to Application Manager and Support Manager.
• Capture user feedback on applications and provide input to Application Change Managers. Actively participate in Application User Groups.
• Proactively review system data and identify training needs or system issues.
• Take part in and where necessary coordinate the writing and review of application training material.
• Participate in system testing by execution of test scripts.
• Other functions as assigned.

 

SUPERVISION

• N/A

 

SECTION 3: EXPERIENCE, SKILLS, KNOWLEDGE REQUIREMENTS

 

• To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.(US)
• Prior relevant experience related to Clinical trials and Clinical applications is preferred.
• The qualified individual should have a good technical knowledge of information systems and database applications.
• Excellent organizational and written skills and the ability to interact with staff at all levels in our organization are essential.
• Excellent communication and customer service skills are essential.

SECTION 4: EDUCATION REQUIREMENTS

 

• Bachelor’s degree or local equivalent preferred, or will have relevant experience for the position

 

Benefits of Working in ICON

Other than working with a great team of smart and energetic people, we also offer a very competitive salary and benefits package that includes an excellent pension scheme, private health care, life assurance and staff recognition schemes. 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

Nurse and patient
Understanding Roles in a Clinical Trial: Sponsors, CROs, and Sites

Teaser label

Industry

Content type

Blogs

Publish date

02/16/2026

Summary

What Sponsors, CROs, and Sites Each Do Clinical research brings together many organisations, each with a specific role in delivering a clinical trial. For those new to the industry, the relationsh

Teaser label

Learn how clinical trials are delivered by understanding the roles of sponsors, CROs, and sites.

Read more
Key skills that make candidates successful in FSP roles

Teaser label

Industry

Content type

Blogs

Publish date

02/16/2026

Summary

Functional Service Provision (FSP), also known as sponsor-embedded delivery, is a core part of how modern clinical research is delivered. At ICON Strategic Solutions, our teams work as an extens

Teaser label

In this blog, we outline the key skills and attributes that help professionals thrive in FSP environments and build long term careers in sponsor-embedded roles.

Read more
Headshot of female
From Lab Bench to Program Leadership: Sinéad McKeon's Career at ICON

Teaser label

Our People

Content type

Blogs

Publish date

02/05/2026

Summary

Building expertise through diverse roles and continuous learning Sinéad McKeon's career at ICON demonstrates how scientific training can evolve into strategic leadership. Now a Senior Manager in Lab

Teaser label

Discover how a career can evolve from hands on lab work to program management in this interview with Sinéad McKeon.

Read more
View all

Similar jobs at ICON

Study Start Up Associate I

Salary

Location

Mexico, Mexico City

Location

Mexico City

Remote Working

Remote

Business Area

ICON Strategic Solutions

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

JR146250

Expiry date

01/01/0001

Rita Villavicencio Read more Shortlist Save this role
Pharmacovigilance Associate/Senior Associate (México City - Hybrid mode)

Salary

Location

Mexico, Mexico City

Location

Mexico City

Remote Working

Hybrid

Business Area

ICON Full Service & Corporate Support

Job Categories

Drug Safety

Job Type

Permanent

Description

We are currently seeking a Pharmacovigilance Associate to join our diverse and dynamic team. As a Pharmacovigilance Associate at ICON, you will play a vital role in monitoring and ensuring the safety

Reference

JR144856

Expiry date

01/01/0001

Florencia Pistolesi Read more Shortlist Save this role
Senior Manager, Site Engagement, Sponsor Dedicated

Salary

Location

US, Sherman Oaks, CA

Location

Los Angeles

Colorado

California

Arizona

Washington

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Study Start Up

Job Type

Permanent

Description

We are seeking a Senior Clinical Site Lead to join a dynamic team working within the client environment.The candidate will be expected to travel to sites on the West Coast of the US. What you will be

Reference

JR145838

Expiry date

01/01/0001

Jamie Pruitt

Author

Jamie Pruitt
Read more Shortlist Save this role
COL/Sr COL

Salary

Location

US, Blue Bell (ICON)

Location

Blue Bell

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for overseeing the planning, execution, and successfu

Reference

JR146216

Expiry date

01/01/0001

Brendan Hoey

Author

Brendan Hoey
Read more Shortlist Save this role
Senior CRA

Salary

Location

Chicago, IL

Location

Indianapolis, IN

Chicago, IL

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.Conducting site visits to assess sit

Reference

JR146514

Expiry date

01/01/0001

Brandon Pupek

Author

Brandon Pupek
Read more Shortlist Save this role
Senior CRA

Salary

Location

US, Raleigh, NC

Location

Raleigh

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.Conducting site visits to assess sit

Reference

JR146510

Expiry date

01/01/0001

Brandon Pupek

Author

Brandon Pupek
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above