JUMP TO CONTENT

Study Support Assistant (Vitória/ES)

  1. Brazil
2025-119862
  1. Clinical Monitoring
  2. ICON Strategic Solutions

About the role

This vacancy has now expired. Please click here to view live vacancies.

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, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.


What you will be doing:

 

The Study Support Assistant will support administrative activities at sponsor's sites. 

 

Pre-screening and screening phase:

  • Support the submission of the protocol and other documents to the ethics committee (EC) for approval and the development and maintenance of files and binders.

During trial conduct:

  • Assist with scheduling patient visits.
  • Transcription of source document datapoints into EDC including query response according to the timelines and which can be clearly accessed in source documents.
  • Submission of applicable trial documents to the ethical and regulatory entities.
  • Archive and maintenance of the regulatory folders and binders.
  • On-site and off-site monitoring visit support, such as communication with CRAs for scheduling visits, providing access to site documentation and supplies to CRA reviews, accommodate meetings with site staff, etc.
  • Audit support, as needed.
  • Manage meetings, as needed.

At closure and follow-up:

  • Support scheduling of follow-up visits.
  • Completion of queries and CRFs in order to achieve DBL in the expected timeline.
  • Support the resolution of any open action item at the site.
  • Support with study close-out visits.

You are:

  • Bachelor's degree in a Science related field.
  • At least 2 years of experience working with administrative activities in clinical trials.
  • Read, write and speak fluent English; fluent in host country language required.
  • Avilability to attent to the site everyday. 
  • Based in Vitória, Espiritu Santo, Brazil. 

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, 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.

https://careers.iconplc.com/reasonable-accommodations

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

List #1

Day in the life

A picture of Suzaita
Suzaita's story - an insight into working in Clinical Research

Teaser label

A Day In The Life

Content type

Blogs

Publish date

04/05/2023

Summary

Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfil

Teaser label

Senior Clinical Research Associate, Suzaita Hipolito, talks about how working in Clinical Research gives her happiness and fulfilment.

Read more
Suzaita Hipolito

by

Suzaita Hipolito

Suzaita Hipolito

by

Suzaita Hipolito

A picture of three people sat down, with a man in focus in the middle
Could you be ICON's next CRA? Yes, and here's how

Teaser label

Career Progression

Content type

Blogs

Publish date

03/20/2020

Summary

Navigating the world of graduate schemes and positions can be daunting, especially if you’re not quite sure of the role or company you want to align yourself with. At ICON, we recognise what a s

Teaser label

Clinical research in the UK has boomed over the last few decades.

Read more
View all

Similar jobs at ICON

Sr Central Monitor

Salary

Location

UK, Livingston

Location

Livingston

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

Job title - Senior Central MonitorLocation - Must be based in the UK Fully sponsor dedicated We are currently seeking a Senior Central Monitor to join our diverse and dynamic team. As a Senior Central

Reference

JR146206

Expiry date

01/01/0001

Amani Yousef

Author

Amani Yousef
Read more Shortlist Save this role
Clinical Research Associate I

Salary

Location

Romania, Bucharest

Location

Bucharest

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking experienced Clinical Research Associates to join our diverse and dynamic FSP team in Romania.  As a Clinical Research Associate at ICON Plc, you will play a critical role in o

Reference

JR143938

Expiry date

01/01/0001

Dariusz Sternlicht Read more Shortlist Save this role
CRA standard

Salary

Location

China, Guangzhou

Location

Guangzhou

Shanghai

Remote Working

Remote or Office

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

JR146671

Expiry date

01/01/0001

Jenny Zhang

Author

Jenny Zhang
Jenny Zhang

Author

Jenny Zhang
Read more Shortlist Save this role
CRA standard

Salary

Location

China, Beijing

Location

Beijing

Remote Working

Remote or Office

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

JR146688

Expiry date

01/01/0001

Jenny Zhang

Author

Jenny Zhang
Jenny Zhang

Author

Jenny Zhang
Read more Shortlist Save this role
Clinical Research Associate

Salary

Location

Slovakia, Bratislava

Location

Bratislava

Remote Working

Remote or Office

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

Job Advert PostingWe are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and a

Reference

JR146875

Expiry date

01/01/0001

Natalia Roth

Author

Natalia Roth
Read more Shortlist Save this role
Clinical Site Associate

Salary

Location

Korea, Seoul

Department

Clinical Monitoring

Real World Solutions

Location

Seoul

Remote Working

Hybrid

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Clinical Site Associate to join our diverse and dynamic team. As a Clinical Site Associate at ICON, you will play a key role in supporting site management activities and ens

Reference

JR146633

Expiry date

01/01/0001

Daisy Park

Author

Daisy Park
Daisy Park

Author

Daisy Park
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above