QA Administrator
About the role
This vacancy has now expired. Please click here to view live vacancies.
Are you a QA specialist or data expert looking for a growth oriented opportunity?
ICON is looking to hire a Quality Assurance Administrator to join their global QA team based in Bangalore, India. This role would really suit someone with excellent business knowledge and a flare for marketing. This role will be primarily preparing information for Senior Management using powerpoint. You will be involved with collating data and interpreting this for the management team.
Key Responsibilities:
- You will effectively provide administrative support to the Quality assurance department especially the QA Management system (iQ)
- iQ Administration support which includes managing the QA and non QA user login accounts and manage project entry to iQ.
- Reporting- regular and adhoc reports for QA management, sponsors and other departments etc.,
- QA Audit support- create, assign and update records as required, create observation records and assist with creation of audit templates.
- QC- perform regular reviews of iQ data to check for inconsistencies and work with QA teams to correct and update records, as needed.
- General QA administration- perform some basic administration tasks for the QA team as needed including organising,scheduling, facilitating meetings etc., and assist in completion of departmental and project goals. Assist with coordination of external audits hosted by the QA department.
Key skills, knowledge and educational requirements:
· Bachelor’s degree in life sciences, business administration or local equivalent qualification/relevant work experience. An M.B.A would be an advantage.
· Prior relevant work experience in Quality assurance, Regulatory, Marketing or other relevance administrative support experience would be ideal.
· Excellent organizational, verbal and written communication skills.
· Strong technical skills, including proficiency in MS Office applications with strong skills in excel.
· Ability to prioritize, multi task and work independently with time sensitive material.
· Able to work independently in a global matrix environment. A strong team player, flexible in work time, if business requires.
· Meticulous attention to detail and excellent customer service skills.
· Thorough understanding of management confidentiality(in relation to both project and personnel information).
· Strong communication skills, both written and oral.
· Ability to produce reports to a high standard will be advantageous.
· Fluency in English is essential.
Benefits
Working for ICON you will be provided with an excellent benefits package and your dedicated recruiter will be able to give you a specific break down at telephone 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, if you are successful you will be invited to an initial telephone interview with one of our dedicated recruiters who will be able to provide you with more details of this opportunity.
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment. *LI-KT1
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. Learn more about Our Culture at ICON
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish 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
Inside ICONContent type
BlogsPublish date
03/15/2026
Summary
Who's Who In a Clinical Trial Team Clinical trials rely on large, cross functional teams working together across countries, time zones and specialisms. For those new to the industry, the number of
Teaser label
IndustryContent type
BlogsPublish date
02/16/2026
Summary
What Sponsors, CROs, and Sites Each Do Clinical research brings together many organisations, each with a specific role in delivering a clinical trial. For those new to the industry, the relationsh
Similar jobs at ICON
Salary
Location
Mexico, Mexico City
Department
Full Service - Development & Commercialisation Solutions
Location
Mexico City
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Permanent
Description
The Site Manager/Start Up Associate I is responsible for assigned project site start-up and qualification activities per study specific requirements. Additionally, the Site Manager/ Start Up Associate
Reference
JR146199
Expiry date
01/01/0001
Author
Olivia MolinaAuthor
Olivia MolinaSalary
Location
Ireland, Dublin
Department
Information technology
Location
Dublin
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Technical Project Management
Non-Clinical Project Management
Job Type
Permanent
Description
We are currently seeking a Senior Project Manager to join our diverse and dynamic team. As a Senior Project Manager, IT at ICON, you will be responsible for leading and managing IT projects, ensuring
Reference
JR142757
Expiry date
01/01/0001
Author
Maya KatsarskaAuthor
Maya KatsarskaSalary
Location
Mexico, Mexico City
Location
Sao Paulo
Bogota
Mexico City
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Scientist
Job Type
Permanent
Description
We are currently seeking a Clinical Scientist to join our diverse and dynamic team. As a Clinical Scientist at ICON, you will play a critical role in designing and conducting clinical studies that adv
Reference
JR146888
Expiry date
01/01/0001
Author
Rita VillavicencioAuthor
Rita VillavicencioSalary
Location
Poland, Warsaw
Location
Warsaw
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
JR146703
Expiry date
01/01/0001
Author
Dagmara DrozdowskaAuthor
Dagmara DrozdowskaSalary
Location
Netherlands, Groningen GRQP
Department
Full Service - Early Clinical and Bioanalytical Solutions
Location
Groningen
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
At ICON, our clinic teams sit right at the heart of Early Phase Clinical Research, where careful planning meets expert clinical execution. As a Clinical Study Manager, you will play a central role in
Reference
JR145931
Expiry date
01/01/0001
Author
Sophia CairnsAuthor
Sophia CairnsSalary
Location
Canada, Burlington
Location
Burlington
Remote Working
Hybrid
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
What you will be doing Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.Maintain and organize clinical trial documentati
Reference
JR145489
Expiry date
01/01/0001
Author
Jonathan HolmesAuthor
Jonathan Holmes