Unternehmen

Contractors

Karriere

Über uns

K-Magazin

Datenschutz

Kontakt

Projekte

Profile

Offene Stellen

Zurück

I would like to be included in the K-Recruiting applicant pool. This will give me the opportunity to receive further exciting offers. By being included in the applicant pool, K-Recruiting GmbH (DE), K-Recruiting LP (US), K-Recruiting Schweiz AG (CH) and K-Recruiting Global AG (CH) will have access to my personal data and will be able to submit offers to me.

The total size of all uploaded files must not exceed 4.4 MB.
Allowed file formats: pdf, pptx, docx, doc, ppt, ods, odt, 7z, gz, rar, zip

Come to k!

I would like to be included in the K-Recruiting contractor pool. This will give me the opportunity to receive further exciting offers. By being included in the contractor pool, K-Recruiting GmbH (DE), K-Recruiting LP (US), K-Recruiting Schweiz AG (CH) and K-Recruiting Global AG (CH) will have access to my personal data and will be able to submit offers to me.

Are you interested in this project?

Schedule a meeting

I would like to be included in the K-Recruiting freelancer pool. This will give me the opportunity to receive further exciting offers. By being included in the freelancer pool, K-Recruiting GmbH (DE), K-Recruiting LP (US), K-Recruiting Schweiz AG (CH) and K-Recruiting Global AG (CH) will have access to my personal data and will be able to submit offers to me.


LEAD ECP-Webseite

Fill out the contact form

Are you interested in this candidate profile?

Nadine Münch

<div class="ck-content" data-wrapper="true" dir="ltr" style="--ck-image-style-spacing: 1.5em; --ck-inline-image-style-spacing: calc(var(--ck-image-style-spacing) / 2); font-family: Arial; font-size: 11pt;">Study Coordinator Oncology (M/W/D)&nbsp;Aufgaben:<ul style="list-style-position: inside;" data-end="827" data-start="459"><li data-end="548" data-start="459">Beratung der Studienleitung bei der Durchführung klinischer Studien (Phase I–IV)&nbsp;</li><li>Eigenständige Recherche in den Patientenakten</li><li><div class="ck-content stickystyles-wrapper-insert" style="--ck-image-style-spacing:1.5em;--ck-inline-image-style-spacing:calc(var(--ck-image-style-spacing) / 2);font-family:Arial;font-size:11pt;" data-wrapper="true" dir="ltr">Koordination und Betreuung von Studienteilnehmer:innen</div></li><li data-end="656" data-start="608">Organisation von Visiten und Studienabläufen</li><li data-end="705" data-start="657">Dokumentation gemäß GCP und Studienprotokoll</li><li data-end="773" data-start="706">Kommunikation mit Monitoren, Prüfer:innen und externen Partnern</li><li data-end="827" data-start="774">Verwaltung studienrelevanter Unterlagen und Daten&nbsp;</li></ul>&nbsp;Qualifikation:<ul style="list-style-position: inside;"><li>Erfahrung im Bereich klinische Studien / Studienkoordination</li><li>Kenntnisse in ICH-GCP und regulatorischen Anforderungen</li><li>Organisationstalent und Genauigkeit</li><li>Gute Deutsch- und Englischkenntnisse</li><li>Idealerweise Erfahrung mit eCRF/RAVE-Systemen</li></ul>&nbsp;Rahmendaten:&nbsp;Start: asap; spätens zum 11/ 2025Dauer:12 MonateAuslastung: 2-3 Tage die WocheEinsatzort: remote &amp; on-site (Linz &amp; Umgebung) in den Prüfzentren&nbsp;</div>