JUMP TO CONTENT

Laboratory Support Coordinator (Data Entry) - Full Time

JR062482

About the role

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

About the Laboratory Support Coordinator role within ICON:

The Laboratory Support Coordinator will select and enter quality control data to support the Global QC Analysts in producing relevant information in order to assure the production of high quality results. Duties include Including, but not limited to, processing and entering data, maintaining spreadsheets, triaging reports and other relevant tasks related to the creation and production of data. They will assist the Global QC Department with Quality monitoring in the lab with duties including; attending, scheduling and taking meeting minutes, setting reminders for important dates, distribution of mail and reports, generating and monitoring reports, placing orders for common stationary supplies and assisting with specific projects. The Lab Support Coordinator will participate in required Continuous Professional Education Programs, including conferences, internal journal club and lectures, as required.

Benefits of working at ICON:

We will provide our Laboratory Support Coordinator with the resources to be successful in supporting their line of business. In addition, we offer a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, vacation, and an annual incentive plan to reward performance.

To succeed you will need:

  • Ability to use and create spreadsheets in Excel
  • Knowledge of Microsoft Office and Outlook
  • Must have excellent oral and written communication skills to be able to effectively communicate to internal lab management and external consultants.
  • Demonstrated ability to manage multiple tasks with good organization skills and good attention to detail.
  • Task oriented demonstrating the ability to handle large work load demands and to trouble shoot issues timely when required.
  • Customer Focused -providing timely, confident, reliable and friendly service to all our internal and external customers.
  • Demonstrated ability to keep accurate, legible records and recognize the need to handle these records and all other information in line with GCP/GLP/GDP.
  • Good communication skills that allow for confident interaction with all levels in the organization.
  • Demonstrates a high level of personal integrity and ethical behavior with a responsible and mature approach to work duties.
  • At least 3 years relevant experience.

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 - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment

List #1

Day in the life

middle aged male wearing shirt
Francis' Journey back to ICON

Teaser label

Our People

Content type

Blogs

Publish date

03/26/2026

Summary

Why Francis returned to ICON: building a long-term career in clinical research Francis Kayamba is a Clinical Research Associate based in Johannesburg, South Africa. He first joined ICON in February

Teaser label

Francis Kayamba shares what drew him back to ICON and how the sponsor-embedded model works.

Read more
Lydia's Journey Back to ICON

Teaser label

Our People

Content type

Blogs

Publish date

03/24/2026

Summary

Career paths are rarely straightforward, especially in the fast moving world of clinical research. For many professionals, gaining experience across organisations can provide valuable perspectiv

Teaser label

Learn about Lydia's return to ICON and why she felt it was a natural choice.

Read more
Headshot image of male
Driving Trials Forward: Study Start-Up Leadership at ICON

Teaser label

Our People

Content type

Blogs

Publish date

03/16/2026

Summary

Driving Study Start-Up: James Pereira's Journey at ICON James Pereira's career in clinical research has been shaped by a single driving question: how do we get studies started faster? From his earl

Teaser label

Explore James Pereira's career in study start-up at ICON, leading global teams to accelerate patient access.

Read more
View all

Similar jobs at ICON

Site Engagement Liaison

Salary

Location

US, Blue Bell (ICON)

Location

Blue Bell

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Patient Recruitment

Job Type

Permanent

Description

We are currently seeking a Site Engagement Liaison to join our diverse and dynamic team. As a Site Engagement Liaison at ICON, you will play a pivotal role in fostering relationships with clinical tri

Reference

JR147677

Expiry date

01/01/0001

Brendan Hoey

Author

Brendan Hoey
Read more Shortlist Save this role
- Global Study Associate (GSA), CVRM

Salary

Location

Bulgaria, Sofia

Location

Sofia

Warsaw

Johannesburg

Barcelona

Madrid

Gdansk

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

We are currently seeking a Global Clinical Trial Associate to join our diverse and dynamic team. The Global Clinical Trial Associate is an integral part of the study team, responsible for providing ad

Reference

JR147034

Expiry date

01/01/0001

Shelley Ball

Author

Shelley Ball
Read more Shortlist Save this role
HEOR Scientist

Salary

Location

US, Blue Bell (ICON)

Location

Raleigh

Blue Bell

Basking Ridge, NJ

Chicago, IL

Seattle, WA

Dallas, TX

Houston, TX

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Medical & Scientific Affairs

Job Type

Permanent

Description

What You Will Be Doing:Strategy Drives sustained integration of HEOR from early clinical development through commercialization depending on focus of role.Develops and oversees HO research strategy for

Reference

JR146217

Expiry date

01/01/0001

Jonathan Holmes Read more Shortlist Save this role
Senior Pharmacovigilance Associate

Salary

Location

India, Chennai

Location

Chennai

Remote Working

Hybrid

Business Area

ICON Full Service & Corporate Support

Job Categories

Drug Safety

Job Type

Permanent

Description

We are currently seeking a Senior Pharmacovigilance Associate to join our diverse and dynamic team. As a Senior Pharmacovigilance Associate at ICON, you will be instrumental in ensuring the safety and

Reference

JR139662

Expiry date

01/01/0001

Archana Bakkiyarajan Read more Shortlist Save this role
CRA

Salary

Location

Taiwan, Taipei

Location

Taipei

Remote Working

Hybrid

Business Area

ICON Strategic Solutions

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

JR145146

Expiry date

01/01/0001

Sandy Tang

Author

Sandy Tang
Sandy Tang

Author

Sandy Tang
Read more Shortlist Save this role
Clinical Site Manager II

Salary

Location

France, Paris

Location

Paris

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical

Reference

JR147407

Expiry date

01/01/0001

Serena Milanesi Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above