CDC II
About the role
This vacancy has now expired. Please click here to view live vacancies.
“At ICON, it's our People that set us Apart”
Are you passionate about improving the quality of human life? If so, we invite you to join us in creating a healthier world tomorrow.
ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development - from compound selection to Phase I-IV clinical studies.
We started as a team of 5 members in 1990 & today we are ranking at top 4 worldwide based on revenue of 2015. Currently we have 12200+ employees across the globe. ICON is a $1.575bn company having its presence across 89 offices in 37 countries.
Position Summary
Serve as a resource tor projects, deliverables. and improvement initiatives in the Data Management department.
Perform data management activities to ensure the generation of accurate, complete, and consistent clinical data, and support timely project delivery to the highest quality.
Ensure all activities are conducted in accordance with Good Clinical Practices (GCP), applicable SOPs, client requirements, and departmental requirements.
Job Responsibility
· *Recognize, exemplify and adhere to ICON's valL}es which centers around our commitment to People. Ciients 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
· *Perform Quatity Reviews and appropriately address all issues.
· *Compile and distribute necessary study documentation and maintain accurate and complete study flies jn accordance with atl applicable procedures.
· 'Identify and appropriately address data discrepancies (n the clinical data via computerized edits and manuat checks/listings.
· *Independently and accurately generate data queries to resolve data discrepancies.
· *Appropriately address responses to data queries and accurately update the clinical data as necessaty.
· *Accurately and consistently apply data handling conventions to Case Report Forms as necessary in accordance with all applicable procedures.
· *Independently and accurately prepare database test documentation and test data entry screens.
· *Assist with the validation of edit check programs.
· *Assist with the development, review, and maintenance of relevant Data Management Study Specific Procedures.
· *Accurately perform Serious Adverse Event reconciliation in accordance with all applicable procedures.
· *Accurately perform external data reconciliation in accordance with all
· applicable procedures. Accurately perform case report form annotation.
· Provide input to, generate and distribute status reports as required, ensuring their accuracy.
· Represent Data Management at internal / external meetings as appropriate.
· Serve as a mentor for other staff in Data Management, and provide input to the performance appraisal process as requested.
· Undertake other reasonably related duties as may be assigned from time to time.
Qualification
Minimum of a Diploma or Degree in a Scientific discipline or locai equivalent. or equivalent work experience as described in Section 3 of this document.
PROCESS
Technical and competency selection:
When you spot an opportunity you’re interested in and submit an application, one of our Talent Acquisition Specialists will contact you to evaluate your suitability for this position, as well as for other openings within the business.
The evaluation will look at your technical skills and your competencies – for example, delivering excellence.
Interview
After this, we’ll let you know if we’ll be progressing with your application. If you have been successful at this stage, we will talk you through a telephone interview. This will then be followed by an interview with our Hiring Manager, either face to face or by tele-conference.
Offer
If you’re successful, we will notify you with details of the offer, talk you through our culture and values, answer any questions you may have – and above all, welcome you to the ICON team.
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
Inside ICONContent type
BlogsPublish date
08/07/2025
Summary
Building a Career at ICON: A Conversation with Susie McEvoy, Senior VP of HR At ICON, career journeys are rarely linear – and Susie McEvoy’s story is a powerful example of that. From joining as a

Teaser label
Inside ICONContent type
BlogsPublish date
08/01/2025
Summary
Clinical Research Nursing: A Vital Career at ICON Clinical research nursing is a specialised discipline that blends expert patient care with the science of clinical trials. Nurses in this role ar
.png)
Teaser label
Inside ICONContent type
BlogsPublish date
07/28/2025
Summary
CTMS: The Essential Tool for Clinical Research Professionals Clinical trials have rapidly evolved, accelerated by technology and digital innovation. Central to this evolution is the Clinical Tria
Similar jobs at ICON
Salary
Location
Argentina
Department
Clinical Trial Management
Location
Argentina
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Clinical Trial Manager you will play a key role in improving the lives of patients by accelerating the development of our customers drugs and devices through innovative solutions.
Reference
2025-121308
Expiry date
01/01/0001
Author
Tulio SanquizAuthor
Tulio SanquizSalary
Location
Argentina
Department
Clinical Trial Management
Location
Argentina
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Clinical Trial Manager you will play a key role in improving the lives of patients by accelerating the development of our customers drugs and devices through innovative solutions.
Reference
2025-121309
Expiry date
01/01/0001
Author
Tulio SanquizAuthor
Tulio SanquizSalary
Location
US, New York, NY, Rochester
Department
Full Service - Development & Commercialisation Solutions
Location
Rochester
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Software Engineer
Job Type
Permanent
Description
We are currently seeking a Software Engineer to join our diverse and dynamic team. As a Software Engineer at ICON, you will play a crucial role in developing and implementing software solutions that e
Reference
JR132906
Expiry date
01/01/0001
Author
Kris CostelloAuthor
Kris CostelloSalary
Location
US, New York, NY, Whitesboro
Department
Full Service - Early Clinical and Bioanalytical Solutions
Location
Whitesboro
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Project/ Program Management
Job Type
Permanent
Description
We are currently seeking a Manager of Project Management at ICON Plc to join our diverse and dynamic team. As the Manager of Project Management, you will be responsible for the overall direction and m
Reference
JR133105
Expiry date
01/01/0001
Author
Hanna PitcairnAuthor
Hanna PitcairnSalary
Location
Denmark
Department
Clinical Monitoring
Location
Denmark
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA in Denmark you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare and assigned to a single sponsor.
Reference
2025-121593
Expiry date
01/01/0001
Author
Alison BurtonAuthor
Alison BurtonSalary
Location
Sweden
Department
Clinical Monitoring
Location
Sweden
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA in Sweden you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare and assigned to a single sponsor.
Reference
2025-121592
Expiry date
01/01/0001
Author
Alison BurtonAuthor
Alison Burton