Clinical research associate Jobs in Erzhausen
Sr. Clinical Research Associate
AvaniaHesse, DEQuality Assurance Associate
MarkenKelsterbach, Germany- Gesponsert
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GSI Helmholtzzentrum für Schwerionenforschung mbHDarmstadt, DeutschlandSenior Research Scientist Molecular Biology
AB EnzymesDarmstadt, DE(Senior) Manager, Medical Science Liaison, Therapy Development, Transcatheter Mitral and Tricuspid Therapies (Germany)
Edwards LifesciencesGermany, Hessen, Remote- Gesponsert
BTA (m / w / d)
GULP Information Services GmbHDarmstadt, Hessen, GermanyResearch Associate (m / f / d), Pharmacometrics
Paul-Ehrlich-InstitutLangen, GermanyAssociate Director Clinical Data Manager (all genders)
Merck KGaA, Darmstadt, GermanyDarmstadt, GermanyResearch Coordinator, Medical (m / f / d)
International SOSNeu-Isenburg, DE, 63263Support Quality Associate
AutodeskDarmstadt, Germany- Gesponsert
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GSI Helmholtzzentrum für Schwerionenforschung GmbHDarmstadt- Gesponsert
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MerckDarmstadt, Hessen, DEBTA (m / f / d)
GULP – experts unitedDarmstadtWarehouse Associate / Lagerlogistik Mitarbeiter
Marken Time Critical Express GmbHKelsterbach, Hessen, Germany- Gesponsert
Clinical Education and Training Specialist (f / m / d)
SprintRay Europe GmbHWeiterstadt bei Darmstadt, Germany- Gesponsert
Post-doctoral researcher - Functional Genomics in AML
Universitätsklinikum FrankfurtDreieichResearch Associate for Software Analysis
Fraunhofer-GesellschaftDarmstadtAssociate Finance 1+
Schollmeyer&SteidlHessenSite Coordinator
Cummins Inc.Gross-Gerau, DEUSr. 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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