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Clinical Trial Coordinator

Clinical Monitoring
ICON Strategic Solutions
Remote
TA Business Partner

• Full Service Division

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About the role

This vacancy has now expired. Please see similar roles below...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

Op zoek naar je eerste stappen in het klinisch onderzoek?
Werken voor 1 sponsor spreekt jou aan?
Je houdt van zelfstandigheid, administratie en opvolging van een project van A-Z
👉 👉 👉 Dit is jouw kans !
ICON plc is op zoek naar een Clinical Trial Coordinator voor een pharma-bedrijf in regio Amsterdam.

ONZE SPONSOR:

Onze sponsor is een Amerikaans farma bedrijf dat vooral actief binnen oncologie. Maar ook andere therapeutische gebieden zoals vaccines, gynaecologie, cardiologie, infectious diseases, hematologie, ... komen aan bod. De studies bevinden zich in fase 2 en 3.

JOUW JOB:

📑 Als Clinical Trial Coordinator ben je verantwoordelijk voor de administratieve opvolging van je studies en ziekenhuis sites.
📒 Je zorgt voor een nauwkeurige opvolging van alle essentiële documenten.
🧾Ook het financiële luik vind je interessant en je werkt mee op budget, contracten en betalingen
📬 Je bent een administratieve duizendpoot die ook het logistieke aspect op zich neemt (zoals de organisatie van meetings, zendingen naar de sites, etc...)

🙋🏼‍♀️ Je wordt toegewezen aan enkele studies, die jij van A-Z nauwkeuring en volgens ICH-GCP opvolgt samen met de CRA en het studie-team

Jouw verantwoordelijkheden omvatten :
archiveren en tracken van essentiële studiedocumenten
labels voorzien voor de te onderzoeken medicatie en studiemateriaal
update van klinische databases
update van handleidingen, document-voorbereiding
bezorgen en verkrijgen van investigator formulieren/lijsten voor evaluatie en validatie van een site, opstart van een site en voor de indieningen
investigator file voorbereiding en up-to-date houden
submissie-paketten voorbereiden voor de goedkeuring van de studie naar authoriteiten
in samenwerking met finance landspecifieke en site budgetten klaarmaken
mee opstellen, onderhandelen en goedkeuren van contracten (Clinical Trial Agreement,...)

JOUW VAARDIGHEDEN:

❤️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 kan je goed uitdrukken in het Nederlands en Engels.
📒 Je kent de basics van ICH-GCP.

ONS AANBOD:

Homebased contract met flexibiliteit om vanuit het kantoor van de klant te werken
Boeiende projecten bij onze sponsor
Veel variatie, veel leermomenten en vooral veel nieuwe uitdagingen
Begeleiding door de sponsor EN icon
Focus op work-life balance
Aantrekkelijk salarispakket met extralegale voordelen

ICON PLC:

Je maakt deel uit van een organisatie die is erkend als een van 's werelds toonaangevende Contract Research Organisations door middel van een aantal high-profile industrie awards.Je komt te werken in zeer betrokken en professionele teams bij de sponsor maar ook binnen ICON plc. Omdat je voor één sponsor kunt werken, krijg je de kans om diepgaande ervaring op te doen. Je wordt ondersteund door onze ICON plc Operations Managers die ervoor zorgen dat je je tijdens je loopbaan bij ICON plc optimaal kunt ontwikkelen.

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


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.

ICON and you

A better career. A better world. A better you.

Our people are our
greatest strength
, are the core of our culture and the
driving force
behind our success. Throughout all levels of the company, our people have a
drive to succeed
and a
passion
that ensures what we do, we do well. We
help you build exciting and rewarding careers
, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an
industry leader
.
List #1
Day in the life
Teaser label
Content type
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.
Teaser label
Content type
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.
Teaser label
Content type
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.
by
Suzaita Hipolito
by
Suzaita Hipolito

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