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Site supervisor • neu anspach
Sr. Clinical Research Associate
AvaniaHesse, DEVIE Platform
ValeoFriedrichsdorfIT Systemadministrator / Fachinformatiker (m / w / d)
PERMACON GmbH FrankfurtFriedrichsdorf, DeutschlandInpatient Registered Nurse – RN – Dialysis
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FRESENIUS_KABIBad Homburg- Gesponsert
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AmadeusBad HomburgFinanzbuchhalter (m / w / d)
Actief Personalmanagement GmbHFriedrichsdorf, TaunusProjektleitung Technik (w / m / d)
Neptuned GmbHNiedernhausen, Hessen, DE(Senior) Manager, Medical Science Liaison, Therapy Development, Transcatheter Mitral and Tricuspid Therapies (Germany)
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ING DeutschlandKronberg, Germany- Gesponsert
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Dorint Hotel Frankfurt / OberurselOberursel, DeutschlandCustomer Service Manager
JLLKronberg im Taunus, DEUTechnical Project Manager, Platform Technologies
PharmaLexBad Homburg- Gesponsert
Sales & Forecast Reporting Specialist •
Nintendo of Europe SEBad HomburgCustomer Service Engineer
Ribbon Communications Operating CompanyOberursel, Hesse, GermanyOffice Coordinator Germany
BioMarinKronberg, GermanySr. Clinical Research Associate
AvaniaHesse, DE- Vollzeit
Avania is hiring Senior Clinical Research Associates (Sr CRAs)
Avania’s ClinOps Team establishes, maintains and supports clinical trials; as a key member of the team, our Sr CRA performs clinical trial oversight for the trials, verifying that the rights and well-being of human subjects are protected, and that reported trial data are accurate, complete, and verifiable (from source documents). Partnering closely with our Trial sites, Avania's Sr CRA ensures that the conduct of the trial follows approved protocols / amendment(s), with ISO14155 or ICH-GCP, and with applicable regulatory requirements.
Our Senior CRA role includes the following key activities -
- Interact with and guide study investigators and study coordinators in conducting clinical trials in accordance with study protocols. Member of a site Start-up Team for assigned projects.
- Monitor site’s completion of action items between visits and help prepare for audits and inspections; conduct and write accurate visit reports in accordance with SOPs and GCP (SQV, SIV, IMV, COV)
- Ensure data entered on the CRFs is timely, accurate and verified. Collaborate with analytical services to obtain clean database, resolve queries and conduct or participate in data reviews (both internally and with sponsor), identifying and communicating trends or erroneous data.
- Participate in internal TMF reviews, as needed.
- Develop and maintain trackers, such as visit reports trackers, site trackers, recruitment and enrollment trackers.
- Review and write informed consent forms. Review of protocols, investigator brochures on compliance with applicable regulations and CRFs in development. Prepare clinical trial agreements and present to site and study sponsor.
- Review regulatory compliance for study documents and protocols.
- May act as a Clinical Lead, overseeing clinical trial activities at investigational sites (will require travel to investigational sites).
Candidates who offer a combination of the skills, knowledge and experience listed below are encouraged to apply. With our continued growth we are hiring talent to join us on our journey and grow with us.
Sr CRAs require skills in planning and preparation; sourcing and collecting information; prioritizing tasks and actions; and displaying a proactive attitude to assist in project planning and study execution.
We seek -
We offer -
We look forward to receiving your application!
When you need to advance your career, it takes Avania!
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