Join Fortrea’s mission to transform clinical trials and improve patient outcomes.
As a
Study Start Up Site Navigator I
in Germany or Austria, you’ll support site activation activities and help ensure smooth collaboration between study teams and clinical sites.
Key Responsibilities
Assist with initial site outreach, including sending feasibility surveys and supporting collection of Confidentiality Agreements.
Support preparation for Remote Pre-Study Visits (PSVs) and help with follow-up documentation such as trip reports and required materials.
Coordinate basic administrative tasks related to contract and budget processes under guidance.
Provide support for regulatory submissions and ethics committee documentation.
Act as a point of contact for routine queries between sites and internal teams.
Track site readiness and escalat any blockers to senior team members.
Maintain accurate records and assist with reporting of start-up metrics.
Must-haves:
Bachelor’s degree in life sciences or a related field (or equivalent experience).
Strong interest in clinical research and willingness to learn and previous experience with study-start up and/or budget and contracts in clinical research.
Basic understanding of ICH-GCP principles.
Good organizational and communication skills.
Fluency in German and English (written and spoken)
Preferred:
Internship or exposure to clinical research or healthcare environment.
Familiarity with MS Office tools; knowledge of eTMF or CTMS is a plus.
What We Offer
Hybrid or remote work options with flexibility.
Comprehensive onboarding and training programs to build your expertise.
Access to Employee Resource Groups (ERGs) and wellness initiatives.
Career development opportunities in a global organization.
Inclusive culture that values diverse perspectives.
#LI-CB1 #LI-Remote #LI-Hybrid
Learn more about our EEO & Accommodations request here.
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Site Navigator I based in Germany or Austria Arbeitgeber: Fortrea
Als Projektkoordinator (mit Fokus auf Budget und Finanzen) in München bieten wir Ihnen die Möglichkeit, in einem kollaborativen und integrativen Arbeitsumfeld zu arbeiten, das auf die Unterstützung klinischer Forschungsoperationen ausgerichtet ist. Unsere Mitarbeiter profitieren von umfangreichen Entwicklungsmöglichkeiten, strukturiertem Onboarding und Schulungen sowie von einem hybriden Arbeitsmodell, das Flexibilität und eine ausgewogene Work-Life-Balance fördert. Bei uns haben Sie die Chance, an bedeutenden globalen klinischen Entwicklungen teilzuhaben und Ihre Fähigkeiten in einem dynamischen Team weiterzuentwickeln.
