Archivist
TA Business Partner
- Full Service Division
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. 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' 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.
The Role:
The Archive Specialist ensures that on-site archive facilities are orderly, secure, and operating within tolerances described in corresponding procedures:
* Ensure that material received for archiving corresponds to that described in submission documentation
* Classify, index, label and store archived records using current inventory system/database
* Retrieve and re-file records as requested by site personnel or visiting auditor/inspector
* Ensure that movement of material in and out of the archives is appropriately documented
* Support sponsor audits and regulatory inspections by performing a review of inventory, retrieving necessary records, and providing a tour of the facility archives, if requested
* Maintain a collaborative relationship with off-site vendor archive contacts
* Manage scheduling of pick-up and deliveries to the facility, monitor associated costs, and make recommendations to Management regarding the vendor relationship
* Manage final record disposition process in an effort to reduce the volume of stored documentation.
* Maintain controlled procedures related to local Records Management
* Facilitate conversion of records to electronic media (e.g., scanning to DVD) for business continuity, space considerations, or convenience
* Complete the necessary document packaging and inventory updates resulting from record conversion. Acts in a proactive, flexible and responsive manner to customer needs
You will need:
* High School diploma or equivalent
* Background in science or GLP regulations desired
* A minimum of 5 years of experience in archival or document control procedures
* Skilled in operating office equipment such as copiers, printers, and scanning machines
* Skilled in operating a personal computer utilizing a variety of software applications
* Strong capacity of assessing and prioritizing multiple tasks and demands in a fast paced environment
* Great at establishing and maintaining cooperative working relationships with others in a team environment
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. Learn more about Our Culture at ICON
Day in the life
Teaser label
IndustryContent type
BlogsPublish 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
Our PeopleContent type
BlogsPublish 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
Our PeopleContent type
BlogsPublish 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
Similar jobs at ICON
Salary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Permanent
Description
As an Informed Consent Specialist II at ICON, you will take a lead role in the development, review, and oversight of informed consent documents for complex, global clinical trials.What You Will Do:You
Reference
JR139377
Expiry date
01/01/0001
Author
Florencia Borello TaianaAuthor
Florencia Borello TaianaSalary
Location
Bulgaria, Sofia
Department
Drug Safety & Pharmacovigilence
Location
Sofia
Warsaw
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Systems
Job Type
Permanent
Description
Senior Clinical System Specialist ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced s
Reference
JR144049
Expiry date
01/01/0001
Author
Caroline LockAuthor
Caroline LockSalary
Location
Bulgaria, Sofia
Location
Sofia
Warsaw
Barcelona
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Contracts Administration
Job Type
Permanent
Description
As a Senior Site Contracts Negotiator at ICON, you will lead the negotiation of clinical trial agreements and budgets with investigator sites, ensuring timely, compliant, and mutually beneficial outco
Reference
JR148451
Expiry date
01/01/0001
Author
Denitsa KrastevaAuthor
Denitsa KrastevaSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Hybrid
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a Clinical Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments an
Reference
JR148387
Expiry date
01/01/0001
Author
Ana TelloAuthor
Ana TelloSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Hybrid
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a Clinical Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments an
Reference
JR148399
Expiry date
01/01/0001
Author
Ana TelloAuthor
Ana TelloSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and a
Reference
JR148396
Expiry date
01/01/0001
Author
Ana TelloAuthor
Ana Tello