JUMP TO CONTENT

Clinical Sample Processor

JR067849

About the role

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

Do you have experience pulling and verifying samples for analysis and final disposition of samples?
Clinical Sample Processor role within ICON:
ICON has a strong reputation in our approaches to clinical development. We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients. We work with top pharmaceutical organizations on emerging therapeutic areas which include but are not limited to Oncology, Vaccines, CNS, Cardiovascular and Pain. We are presently in over 40 countries with over 80 offices worldwide and over 10K employees globally.
The Clinical Sample Processor will provide support to shipping and receiving administrators, log-in biological samples, compare to manifest and assign identification numbers. Maintain sample storage records, determine duplicate samples, determine discrepancies/prepare discrepancy reports and maintain up to date lot listings in study binder.
Benefits of working at ICON:
In addition to partnering with the top pharmaceutical and biotech companies in the world we offer a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, bonus plans, vacation, and other incentives.
To succeed you will need:
We are seeking candidates with a high school degree or equivalent.
To be successful you will be expected to have strong attention to detail, be able to work in a fast paced environment with the willingness to handle bio hazardous samples after training and while using Universal Precautions and personal protective equipment. Must have strong keyboarding/spreadsheet/computer skills.
We invite you to review our opportunities at www.iconplc.com/careers.
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

Heartbeat vitals on monitor
Central Monitoring vs On Site Monitoring

Teaser label

Industry

Content type

Blogs

Publish date

04/03/2026

Summary

Understanding Central Monitoring vs On Site Monitoring Monitoring is a core component of clinical trial oversight. It ensures that studies are conducted in line with the protocol, that data is re

Teaser label

Learn the difference between central monitoring and on site monitoring and how both support patient safety and data quality.

Read more
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
View all

Similar jobs at ICON

Clinical Research Associate

Salary

Location

Thailand, Bangkok

Location

Bangkok

Remote Working

Remote or Office

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

JR148154

Expiry date

01/01/0001

Daisy Park

Author

Daisy Park
Daisy Park

Author

Daisy Park
Read more Shortlist Save this role
Informed Consent Specialist

Salary

Location

India, Bangalore

Location

Bangalore

Chennai

Trivandrum

Bengaluru

Remote Working

Hybrid

Business Area

ICON Full Service & Corporate Support

Job Categories

Study Start Up

Job Type

Permanent

Description

We're currently seeking an Informed Consent Form (ICF) Specialist to join our diverse and dynamic team. As an ICF Specialist at ICON, you'll be crucial in ensuring the accuracy, compliance, and timely

Reference

JR146421

Expiry date

01/01/0001

Kashifa Tahseen Read more Shortlist Save this role
Senior Clinical System Designer

Salary

Location

India, Bangalore

Location

Bangalore

Bengaluru

Remote Working

Remote or Office

Business Area

ICON Strategic Solutions

Job Categories

Clinical Systems

Job Type

Permanent

Description

ICON plc is seeking an experienced Senior Clinical System Designer to join our Clinical Data Management team. In this role, you will be responsible for end‑to‑end Electronic Data Capture (EDC) study b

Reference

JR147762

Expiry date

01/01/0001

Abhisikta Mishra Read more Shortlist Save this role
Accounts Receivable Associate

Salary

Location

India, Chennai

Location

Chennai

Remote Working

Hybrid

Business Area

ICON Full Service & Corporate Support

Job Categories

Accounting & Finance

Job Type

Permanent

Description

Accounts Receivable Associate (Billing)Location : ChennaiWe are currently seeking an Accounts Receivable Associate (Billing) to join our diverse and dynamic team. The Accounts Receivable Associate wil

Reference

JR148256

Expiry date

01/01/0001

Shrayashi Ghosh Read more Shortlist Save this role
Site Specialist

Salary

Location

India, Bangalore

Location

Bangalore

Chennai

Bengaluru

Remote Working

Hybrid

Business Area

ICON Full Service & Corporate Support

Job Categories

Study Start Up

Job Type

Permanent

Description

We are currently seeking a Site Specialist I to join our dynamic team.As a Site Specialist II, you will be responsible for supporting site activation activities, vendor coordination, and documentation

Reference

JR146884

Expiry date

01/01/0001

Nandhini Selvakumar Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above