Jobs 251 bis 260 von 1.262 (dupliziert 1.114)
PharmiWeb - Beelitz
reporting Ensuring company complies with all additional legal and regulatory requirements Assist with special projects and additional controller duties as needed Requirements A Bachelors/Master’s degree inVor 60+ Tage
PharmiWeb - Munich
studies, and strategies including the clinical, regulatory , scientific, operational, and commercial aspects of drug development. Uses knowledge to the organization’s advantage; generates new ideas and enables the organization toVor 60+ Tage
PharmiWeb - Munich
the clinical, regulatory , scientific, operational, and commercial aspects of drug development. Uses knowledge to the organization’s advantage; generates new ideas and enables the organization to improve business performanceVor 60+ Tage
PharmiWeb - Marburg an der Lahn
and Clinical Bioanalytics (RCB) department of CSL Behring Research. The facility provides regulatory compliant bioanalytical assays for the analysis of samples derived samples derived from early phase up to late stageVor 60+ Tage
PharmiWeb - Hessen
construction project. Must have knowledge of German regulations and experience with regulatory training. German language, professional standard. Apply now: If you are interested in learning more or applying to thisVor 60+ Tage
PharmiWeb - Munster
technicians, and to ensure accuracy and compliance with protocols, SOP's and client expectations of quality histotechnology. Sound knowledge of Animal Protection Law, GLPs and regulatory agency guidelines. Excellent verbalVor 60+ Tage
CRA II or SCRA home-based / dedidated to sponsor
PharmiWeb - Munich
protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements Ensure the integrity of the data submitted on Case ReportVor 60+ Tage
Clinical Research Associate with Oncology experience
PharmiWeb - Munich
procedures and protocol requirements are adhered to according to the applicable regulatory requirements Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful sourceVor 60+ Tage
Senior Project Data Manager - Homebased
PharmiWeb - Köln
knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs, especially as related to data handling and processing. Company At Labcorp, we believe inVor 60+ Tage
Clinical Research Associate or Senior Clinical Resea...
PharmiWeb - Munich
of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements Ensure the integrity of the data submitted on Case Report FormsVor 60+ Tage