JUMP TO CONTENT

Validation Analyst

009900_2

About the role

This vacancy has now expired. Please see similar roles below...

DEPARTMENT: Global Data Technologies
JOB TITLE: Validation Analyst I
REPORTS TO: Manager or designee

POSITION SUMMARY

Provide testing support specializing in test script writing, execution, and documentation.

 

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 2%) domestic and/or international
• Conduct testing activities according to relevant ICON SOP’s and appropriate regulations.
• Write and execute formal test scripts and complete associated documentation and ensure test results are reported accurately.
• Complete test script writing and execution for simple to moderate complexity systems.
• Communicate with lead/manager and/or project team regarding system testing progress and issues.
• Complete assigned tasks within timeline constraints and report any quality issues to lead or manager in a timely manner.
• Other responsibilities may be assigned as required.

SUPERVISION

• Participate in mentoring/training other staff members as required.

 

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/LATAM/CAN: minimum 2.5 years of experience in software testing.
• EU/APAC: minimum 2.5 years of experience in software testing.
• Successfully manage multiple tasks and timelines.
• Liaise professionally with team members and system users.
• Basic understanding of SQL and database concepts.
• Knowledge in Test Automation Tools.
• Perform assigned tasks with minimal supervision.
• Strong verbal and written communication skills

EDUCATION REQUIREMENTS

• Bachelor’s degree, or local equivalent, in information systems, science, or related discipline or relevant experience.

 

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

Wooden blocks with the letters SOP
Clinical Research Abbreviations: Essential Terms Explained

Teaser label

Industry

Content type

Blogs

Publish date

11/19/2024

Summary

Decoding Clinical Research Abbreviations: Essential Terms Explained Clinical research professionals use hundreds of abbreviations every day. Simple letters like AE mean Adverse Event, while longer

Teaser label

Discover the must-know abbreviations in clinical research with our easy-to-understand guide.

Read more
5 different images of lab technicians
How to become a Clinical Research Associate (CRA)

Teaser label

Our People

Content type

Blogs

Publish date

11/13/2024

Summary

How to Become a Clinical Research Associate:   A Step-by-Step Guide The clinical research industry is projected to reach $52.0 billion by 2026, growing at an impressive rate of 5.6% annually. This

Teaser label

Explore the step-by-step guide on how to become a Clinical Research Associate (CRA).

Read more
Stethoscope on keyboard
How to Build a Career Path in Clinical Data Management

Teaser label

Career Progression

Content type

Blogs

Publish date

11/12/2024

Summary

Building a Career in Clinical Data Management Clinical data management roles and responsibilities have become increasingly crucial in modern healthcare research and development. The healthcare ind

Teaser label

Discover essential steps to build a successful career path in Clinical Data Management.

Read more
View all

Similar jobs at ICON

Principal Medical Writer

Salary

Location

Belgium, United Kingdom, Denmark, France, Spain, Germany, Netherlands, Switzerland

Department

Medical Affiars & Medical Writing Roles

Location

Belgium

Denmark

France

Germany

Netherlands

Spain

Switzerland

UK

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Medical Writing

Job Type

Permanent

Description

As a Principal Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. As principal medical writer, you will be

Reference

2023-103952

Expiry date

01/01/0001

Natalia Roth

Author

Natalia Roth
Read more Shortlist Save this role
Clinical Trial Assistant

Salary

Location

India, Chennai

Location

Chennai

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Trial Support

Job Type

Permanent

Description

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech

Reference

JR120814

Expiry date

01/01/0001

Nandhini Selvakumar Read more Shortlist Save this role
CTA

Salary

Location

Turkey

Department

Clinical Monitoring

Location

Turkey

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a CTC (Supply) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Reference

2024-115187

Expiry date

01/01/0001

Tuba Su

Author

Tuba Su
Tuba Su

Author

Tuba Su
Read more Shortlist Save this role
Clinical Research Associate I - Academy

Salary

Location

Argentina

Department

Clinical Monitoring

Location

Argentina

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

The Clinical Research Associate monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the prot

Reference

2024-115122

Expiry date

01/01/0001

Tulio Sanquiz

Author

Tulio Sanquiz
Read more Shortlist Save this role
Clinical Research Associate I - Academy

Salary

Location

Argentina

Department

Clinical Monitoring

Location

Argentina

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

The Clinical Research Associate monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the prot

Reference

2024-115120

Expiry date

01/01/0001

Tulio Sanquiz

Author

Tulio Sanquiz
Read more Shortlist Save this role
Operational Compliance Associate II

Salary

Location

US, Winston-Salem, NC, 27104

Location

Winston-Salem

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Operations

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 It

Reference

JR125983

Expiry date

01/01/0001

Sasha Brown

Author

Sasha Brown
Sasha Brown

Author

Sasha Brown
Read more Shortlist Save this role

Browse popular job categories below or search all jobs above