JUMP TO CONTENT

Study Start-up Clinical Research Associate

  1. Amsterdam
2024-115133
  1. Clinical Monitoring
  2. ICON Strategic Solutions
  3. Remote

About the role

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.


Voor 1 van z'n sponsors, based in Amsterdam is ICON op zoek naar een Study Start Up Clinical Research Associate.

Als SSU CRA ben je verantwoordelijk voor het hele proces voor 'green light'.

 

Waar houdt onze sponsor zich mee bezig? 💊

 

Onze partner doet onderzoek in verschillende therapeutische domeinen zoals immunologie, solide tumoren, ophthalmologie, respiratoir, dermatologie, cel- en gentherapie, hematologie, neurologie en hart- en vaatziekten. Het gaat om alle klinische fases van geneesmiddelonderzoek.

 

Wat houdt je job precies in:

 

Als SSU CRA ben je verantwoordelijk voor de relaties met de sites. Je zorgt voor een duurzame start van de studie. De Study Start-Up CRA selecteert de sites en coordineert de opstartactiviteiten:

 

  • Je ondersteunt de nationale SSU strategie
  • Je coordineert start up activiteiten om ervoor te zorgen dat timelines en deliverables worden gehaald.
  • Verantwoordelijk voor tijdige opstartactiviteiten vanaf de toewijzing van het land tot aan de greenlight van de site.
  • Voert bezoeken voor siteselectie uit, controleert of de site in aanmerking komt voor een specifieke studie
  • Belangrijkste contactpersoon voor onderzoekslocaties tijdens de selectie van de locatie, het opstarten van de studie en de indieningen
  • Verzamelt indiening van relevante locatie-specifieke documenten
  • Ondersteunt de voorbereiding van financiële contracten
  • Werkt alle systemen voortdurend bij tot de site groen licht krijgt
  • Ondersteunt de voorbereiding van audits en inspecties, indien van toepassing

 


Naar wie zijn wij op zoek?

 

  • Jij hebt een hart voor klinische studies, dat merkt iedereen aan de gedrevenheid en het enthousiasme die jij elke dag laat zien. Je passie voor je vak ontdekte je tijdens je Bachelor of Master in biomedische wetenschappen, verpleegkunde, geneeskunde, kinesitherapie of een andere gerelateerde richting.  Je hebt minimaal 3 jaar werkervaring in het monitoren van klinische studies. Je kan je goed uitdrukken in het Nederlands en Engels

 

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.

Our benefits examples include:

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others



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

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. 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, 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.

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.

 

#LI-IB4

#Hybride

 

List #1

Day in the life

A picture of Debora Oh
How to excel as a CRA in a Clinical Research Organisation

Teaser label

Our People

Content type

Blogs

Publish date

08/29/2023

Summary

To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her

Teaser label

Brazil-based CRA II Debora Oh shares her tips on how to become a great CRA and provides insight into life at ICON.

Read more
A picture of Yemi Moses
Progressing as a CRA with ICON

Teaser label

Our People

Content type

Blogs

Publish date

05/23/2023

Summary

How to progress as a Clinical Research AssociateTo thrive as a Clinical Research Associate (CRA), it is imperative to cultivate a multifaceted skill set and demonstrate unwavering commitment to exce

Teaser label

 Senior CRA Yemi Moses recounts her development and shares her career ambitions with ICON plc.

Read more
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 fulfilled?

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

View all

Similar jobs at ICON

CRA I

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 CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Reference

2024-115199

Expiry date

01/01/0001

Tuba Su

Author

Tuba Su
Tuba Su

Author

Tuba Su
Read more Shortlist Save this role
CRA II or Senior CRA

Salary

Location

South Africa, Johannesburg

Department

Clinical Monitoring

Location

Johannesburg

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a CRA II or Senior CRA with Oncology experience to join our diverse and dynamic team. As a CRA at ICON, you will play a pivotal role in designing and analyzing clinical trials

Reference

JR125230

Expiry date

01/01/0001

Denitsa Krasteva Read more Shortlist Save this role
CRA II

Salary

Location

Brazil

Department

Clinical Monitoring

Location

Brazil

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

A Clinical Research Associate is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. You

Reference

2024-115131

Expiry date

01/01/0001

Bruna Duarte

Author

Bruna Duarte
Read more Shortlist Save this role
Clinical Research Associate

Salary

Location

Colombia

Department

Clinical Monitoring

Location

Colombia

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will be part of an innovative and

Reference

2024-115229

Expiry date

01/01/0001

Magda Obregon

Author

Magda Obregon
Read more Shortlist Save this role
CRA II and Senior CRA

Salary

Location

US, Portland, OR

Department

Clinical Monitoring

Location

Portland

Blue Bell

Remote Working

Hybrid: Office/Remote

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Senior CRA to join our diverse and dynamic team. As a Senior Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, in

Reference

JR125304

Expiry date

01/01/0001

Meris Myers

Author

Meris Myers
Meris Myers

Author

Meris Myers
Read more Shortlist Save this role
Clinical Research Associate 2

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

2024-114775

Expiry date

01/01/0001

Tulio Sanquiz

Author

Tulio Sanquiz
Read more Shortlist Save this role

Browse popular job categories below or search all jobs above