TA Business Partner
- Icon Strategic Solutions
About the role
As a Clinical Trial Assistant you will be dedicated to one of our global pharmaceutical clients; with whom ICON shares a culture of innovation, flexibility and a common vision of bringing life-improving drugs to market. Leading by example, you can set the standard of excellence and enjoy a challenging career in our exclusive programs.
We are currently looking for a Clinical Trial Assistant to join one of our sponsor-dedicated teams in Issy-les-Moulineaux (2 days office based).
The Clinical Trial Assistant assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives. As a Clinical Trial Assistant you will have the opportunity to experience the full lifecycle of a project and genuinely contribute to drug development and improving patients’ lives.
Key responsibilities include:
- Trial Master File (TMF) creation and management
- Co-ordinate entry and maintain local data into study management systems including setting up new studies
- Ensure collection, review, track and provision of appropriate clinical documents to support regulatory submission
- Track and maintain adequate study related supplies in the office and facilitate their distribution to sites, including preparing and distributing Study File Binders and Site Initiation presentations/materials
- Process, reconcile, distribute and track essential documents and submit them to local archive in compliance with SOPs
- Complete tracking documentation as applicable including but not limited to spreadsheets, study and contract tracker
- Prepare and review site communication documents
- Set-up/maintain courier accounts and organize shipments
You will need:
- A first stable experience as a CTA in Pharma or CRO
- Excellent organization skills
- Ability to work well in a dynamic environment and able to prioritize and respond to changing needs of the business
- Strong IT skills
- Strong communication with the ability to multitask and work effectively under pressure
- Fluency in French and professional proficiency in English
#LI-KD1
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

Teaser label
Inside ICONContent type
BlogsPublish date
01/26/2023
Summary
The CRO market has seen an unmistakable uplift in demand for its services in recent years. The call for personalised medicine, pricing pressures, and increasing complexity in clinical trials are j

Teaser label
Inside ICONContent type
BlogsPublish date
10/03/2022
Summary
In traditional clinical trials, patients must attend regular check-ins at hospitals or clinics but fully remote decentralised clinical trials (DCTs) and hybrid trials limit this by replacing the in-pe

Teaser label
Inside ICONContent type
BlogsPublish date
05/22/2022
Summary
Having enjoyed steady growth over the last several years, it’s predicted that the global clinical trials market will hit a value of $65.2 billion by 2025, and around 58% of this can be attributed to r
Similar jobs at ICON
Salary
Location
Lithuania
Department
Clinical Operations Roles
Location
Lithuania
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
Services/deliverables include the management of all documents and logistical and administrative tasks related to trial feasibility, start-up, execution and close out of clinical trials. Ensures trial
Reference
2025-121989
Expiry date
01/01/0001
Author
Michal CzyrekAuthor
Michal CzyrekSalary
Location
Italy, Milan
Department
Clinical Monitoring
Real World Solutions
Location
Milan
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
Job Type
Temporary Employee
Description
We are currently seeking an Intern to join our diverse and dynamic team. As an Intern at ICON, you will have the opportunity to gain hands-on experience in a professional environment, supporting vario
Reference
JR134149
Expiry date
01/01/0001
Author
Sophie BinghamAuthor
Sophie BinghamSalary
Location
Brazil, Sao Paulo
Location
Sao Paulo
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking a CTA to join our diverse and dynamic team. As a CTA at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex m
Reference
JR132971
Expiry date
01/01/0001
Salary
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
We are currently seeking a CTA to join our diverse and dynamic team. As a Clinical Trial Assistant at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, i
Reference
JR132959
Expiry date
01/01/0001
Salary
Location
France
Department
Clinical Operations Roles
Location
France
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We're hiring a Contract Analyst I for a client-dedicated, home-based role in France.
Reference
2025-121084
Expiry date
01/01/0001
Author
Katrien DoomsAuthor
Katrien DoomsSalary
Location
Poland, Warsaw
Department
Clinical Monitoring
Location
Warsaw
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking an IHCRA (In-House Clinical Research Associate) to join our diverse and dynamic team. As an IHCRA at ICON, you will play a pivotal role in supporting the execution and managem
Reference
JR131538
Expiry date
01/01/0001
Author
Tereza SvobodovaAuthor
Tereza Svobodova