Gbl Data Serv Support Spec I
Talent Acquisition Business Partner
- Full Service Division
About the role
This vacancy has now expired. Please click here to view live vacancies.
Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That's our vision. We're driven by it. And we need talented people who share it.
If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.
To work within the ICOLABS system to add, remove; update users and user accounts for different protocols. To use strong communication, organization, and prioritization skills in functioning as the SME of the ICOLABS system.
In addition, the GDS Data Services Support Specialist II is expected to creating data batches in both basic and custom data formats, completing Quality Control checks, and transmitting data files. Work closely with the GDS NY team to ensure issues are taken care off in a timely manner and completed to the satisfaction of the client/data representative.
To use strong communication, organization, and prioritization skills in functioning as the off-site Global Data Services Support specialist.
Promotion to a GDS Data Services Specialist II will be possible once all requirements for the Data Specialist I position have been met (as deemed by the GDS management team) and have been in the position for a minimum of 2 years.
JD in Details
- Recognize, exemplify and adhere to ICON's values which center 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 10%) domestic and/or international.
- To create, QC, and transmit protocol specific data files in standard data formats in accordance with client specifications and departmental procedures. To help support any part of this process for any other member of the Global data Services team.*
- To work with the Project Management team and external clients on adding, removing, updating and troubleshooting ICOLABS users and user accounts for various protocols in according to GDS ICOLABS SOP's. To check and document blinding QC of studies setup by other members of the Global Data Services team.*
- To create, QC, and transmit protocol specific data files in custom data formats in accordance with client specifications and departmental procedures. To help support any part of this process for any other member of the Global data Services team.*
- Work on QAT requests so ensure that the ICL database has been setup correctly by the setup team. All issues, questions, comments, suggestions should be properly managed and addressed - communication is essential*
- Perform edit checks on lab data using different applications as designated by GDS Management.*
- To help and assist other staff members of the Global Data Services team in any part of the data creation and loading process to help make the overall data transfer process as efficient as possible.*
- Create, QC and send data files in both a standard and custom data format*
- To setup studies in ICOLABS which includes the setup of studies, additions, modification and removing of ICOLABS users.*
- To QC data files and ICOLABS setup in accordance with GDS SOP's for any member of the Global Data Services team*
- To troubleshoot data load issues into ICOLABS and to work with ICOLABS support and or Client Services to resolve issues*
- Perform edit checks to monitor lab data for cleanliness and validity *
- Work on Remote lab data setup, upload results, check for issues, etc.*
- Work on QAT requests from the ICL database setup team, find and notify team of any issues, questions or comments*
- Any other relevant task designated by GDS Management.
Benefits of Working in ICON:
Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON
Day in the life
.png)
Teaser label
IndustryContent type
BlogsPublish date
04/22/2025
Summary
What is an IND or NDA? A Guide for Aspiring Clinical Research Professionals If you’re considering a career in clinical research or the broader pharmaceutical and biotech industry, you’ve likely c
.png)
Teaser label
IndustryContent type
BlogsPublish date
04/22/2025
Summary
When it comes to clinical trials, one of the most important documents you’ll hear about is the Informed Consent Form (ICF). Whether you're starting out in clinical research or exploring job opportunit
.png)
Teaser label
IndustryContent type
BlogsPublish date
04/17/2025
Summary
CRA vs CRC Embarking on a career in clinical research is an exciting journey for STEM graduates, offering opportunities to contribute directly to the development of new therapies and to safeguard
Similar jobs at ICON
Salary
Location
Chile
Department
Clinical Trial Management
Location
Chile
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Clinical Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will be part of an innovative and globa
Reference
2025-118938
Expiry date
01/01/0001
Author
Magda ObregonAuthor
Magda ObregonSalary
Location
Puerto Rico
Department
Project Management Roles
Location
Puerto Rico
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Project Management
Job Type
Permanent
Description
As a Project Manager 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 global phar
Reference
2025-118937
Expiry date
01/01/0001
Author
Magda ObregonAuthor
Magda ObregonSalary
Location
Mexico
Department
Biometrics Roles
Location
Mexico
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Data Management
Clinical Data Scientist Lead
Clinical Systems
Data Standards Consultant
Job Type
Permanent
Description
As a Senior Clinical Data Coordinator (Sr CDC) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Working within one of ou
Reference
2025-118936
Expiry date
01/01/0001
Author
Magda ObregonAuthor
Magda ObregonSalary
Location
United States
Department
Regulatory, Drug Safety/ Quality Assurance & Other roles
Location
United States
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Other
Job Type
Permanent
Description
As a Sr. TAT Expert you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-118429
Expiry date
01/01/0001
Author
Melissa BennerAuthor
Melissa BennerSalary
Location
Bogota
Department
Clinical Trial Management
Location
Bogota
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Clinical Trial Manager 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 glo
Reference
2025-118470
Expiry date
01/01/0001
Author
Magda ObregonAuthor
Magda ObregonSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own I
Reference
JR129630
Expiry date
01/01/0001
Author
Ana LuciaAuthor
Ana Lucia