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Health coordinator Jobs in Steinenbronn
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Health coordinator • steinenbronn
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Clinical Project Coordinator
PharmiwebStuttgart, DE- Gesponsert
Business Management Coordinator (M / W / D)
Lapp GroupStuttgart, Germany- Gesponsert
Internship in Digital Experience Center Coordinator
Bosch GroupStuttgart, Baden-Württemberg, Germany- Gesponsert
Office Coordinator / Bürokoordinator - Office Management (m / w / d)
Gleiss LutzStuttgart, DeutschlandFibre Design Coordinator
CyientStuttgart, GermanyBankett Coordinator
Hilton Hotel Garden Inn Stuttgart-NeckerparkStuttgartQuality Coordinator Germany
World Courier (Deutschland) GmbHStuttgart, GermanyVDC Coordinator, (m / w / d)
CRBBöblingen, BW, DESite Coordinator - Stuttgart, Germany
Magellan Health ServicesStuttgart, , GermanyHR Coordinator (w / m / d)
HUGO BOSSMetzingen, DEMeeting & Event Coordinator
Mövenpick Hotel Stuttgart AirportStuttgartWHS Coordinator (m / w / d)
Amazon SZ Wolfhagen GmbHStuttgart, DESales Coordinator (m / w / d)
collective mind GmbHLeonberg, Baden-Württemberg, GermanyWHS Coordinator (m / w / d)
Amazon Deutschland S38 Transport GmbH - L98Stuttgart, DEWHS Coordinator (m / w / d)
Amazon Deutschland W12 Transport GmbH - J53Stuttgart, DESite Security Coordinator
Amentum70563 Stuttgart, Germany- Gesponsert
Communications & Event Coordinator (m / w / d)
Holtzbrinck Publishing GroupStuttgart, DeutschlandProject Coordinator (m / f / d)
GULP – experts unitedStuttgartClinical Project Coordinator
PharmiwebStuttgart, DEDue to continuous business growth and a strong study pipeline, we are currently looking to hire Project Coordinators to join our successful and growing German team and engage in clinical trial management on a day-to-day level. This position will work with our operational teams to accomplish tasks and projects that are instrumental to the company’s success.
Responsibilities
- Work closely with the Project Clinical Trial Manager for timely delivery of recurrent tasks consistently with a high degree of accuracy;
- Compile and maintain project-specific status reports within the Clinical Trial Management System (CTMS);
- Interact with the internal project team, Sponsor, study sites, and third-party vendors;
- Ownership of the Trial Master File;
- Manage initial and ongoing site supply shipments;
- Create and maintain project timelines and enrolment projections; and
- Coordinate project meetings and produce quality minutes.
Qualifications
Medpace Overview
Medpace is a full-service clinical contract research organisation (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks
Awards
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
EO / AA Employer M / F / Disability / Vets