01.06.24 | Vollzeit | Frankfurt am Main | PharmiwebStart Up Team, you will play an integral role in making sure that physicians at our research sites are prepared to start the trial of investigational, new pharmaceutical and biological products for clinical trials at their local practices. The Role • To review and negotiate clinical site investigator
Später ansehen23.05.24 | Vollzeit | Tübingen | CureVac Corporate Services GmbHThe versatile biological molecule for medical purposes. Our focus is on prophylactic vaccines, innovative cancer immunotherapies, and protein-based therapies. All RNA people are striving to achieve our main joint goal To bring multiple best-in-class mRNA medicines to market. To strengthen our team in Tübingen
Später ansehen28.05.24 | Vollzeit | Wiesbaden | CureVac Corporate Services GmbHThe versatile biological molecule for medical purposes. Our focus is on prophylactic vaccines, innovative cancer immunotherapies, and protein-based therapies. All RNA people are striving to achieve our main joint goal To bring multiple best-in-class mRNA medicines to market. To strengthen our team in Tübingen
Später ansehen23.05.24 | Vollzeit | Bad Homburg | Fresenius Medical Carebiological safety assessment according to ISO 10993-1 Secondary Tasks - Support regulatory compliance, speed to market, reduction of risks to patients resulting in an increase in overall user satisfaction and enhanced regulatory compliance (as member of CFT or extended sub-teams) - Support a Design Control
Später ansehen01.06.24 | Vollzeit | Wiesbaden | palleos healthcare GmbHData Manager (Bioinformatiker, Informatiker oder Naturwissenschaftler) (m/w/d) Palleos Healthcare, eine Full-Service-CRO aktiv in der DACH-Region, etabliert sich in der europäischen klinischen Forschungslandschaft. Als Teil der Xlife Sciences Gruppe zielen wir darauf ab, Forschungsprojekte und Biote
Später ansehen24.05.24 | Vollzeit | Bad Homburg | Fresenius Medical Carebiological safety assessment according to ISO 10993-1 Secondary Tasks - Support regulatory compliance, speed to market, reduction of risks to patients resulting in an increase in overall user satisfaction and enhanced regulatory compliance (as member of CFT or extended sub-teams) - Support a Design Control
Später ansehen01.06.24 | Vollzeit | Dreieich | CytivaBe part of something altogether life-changing!Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medi
Später ansehen30.05.24 | Vollzeit | Bad Homburg | Fresenius Medical Care AG & Co. KGaAStatements) - Acting as sponsor, study monitor and contact for chemical/biocompatibility studies in internal and external laboratories (creation of test plans and test reports) - Compilation of overall biological safety assessment according to ISO 10993-1 Secondary Tasks - Support regulatory compliance
Später ansehen30.05.24 | Vollzeit | Bad Homburg | Fresenius Medical Care AG & Co. KGaAAs sponsor, study monitor and contact for chemical/biocompatibility studies in internal and external laboratories (creation of test plans and test reports) - Compilation of overall biological safety assessment according to ISO 10993-1 Secondary Tasks - Support regulatory compliance, speed to market
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