23.05.24 | Vollzeit | Mainz | www.actief-personal.deSachbearbeiter (m/w/d). This is what you can expect from us - Secure job with permanent employment contract - Concrete chance of being taken on - Attractive salary package according to BAP tariff - Vacation and Christmas bonus - Home office possible - Flexible working hours from 0630 - 1830 Your tasks
Später ansehen23.05.24 | Teilzeit, Vollzeit | Mainz | www.actief-personal.deSachbearbeiter (m/w/d) in Arbeitnehmerüberlassung. This is what you can expect from us - Secure job with permanent employment contract - Concrete chance of being taken on - Attractive salary package according to GVP tariff - Entlohnung in höchster Stufe 25,88 €/Stunde - Personal support from our competent team
Später ansehen23.05.24 | Vollzeit | Johanniskirchen | www.actief-personal.deFor you as a Production Planner (m/f/d). This is what you can expect from us - Home office possible - Flexible working hours - Secure job with permanent employment contract - Concrete chance of being taken on - Attractive salary package according to GVP tariff - Vacation and Christmas bonus Your tasks
Später ansehen23.05.24 | Vollzeit | Münster | www.actief-personal.deAre looking for exactly you as an employee in internal sales (m/f/d). This is what you can expect from us - Secure job with permanent employment contract - Attractive salary package according to BAP tariff - Vacation and Christmas bonus - Long-term employment in a renowned company in the region - Personal
Später ansehen22.05.24 | Vollzeit | Ludwigshafen am Rhein | BioNTech SEPublications Experience in leading to answer health authority questions (FDA, EMA) and leading in statistics on regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian
Später ansehen22.05.24 | Vollzeit | Mainz | BioNTech SEPublications Experience in leading to answer health authority questions (FDA, EMA) and leading in statistics on regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian
Später ansehen22.05.24 | Vollzeit | Frankfurt am Main | BioNTech SEPublications Experience in leading to answer health authority questions (FDA, EMA) and leading in statistics on regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian
Später ansehen22.05.24 | Vollzeit | Worms | BioNTech SEPublications Experience in leading to answer health authority questions (FDA, EMA) and leading in statistics on regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian
Später ansehen22.05.24 | Vollzeit | Mainz | BioNTech SEPublications Experience in leading to answer health authority questions (FDA, EMA) and leading in statistics on regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian
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