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Demonstrate proficiency and understanding of all aspects of the approved DurAVR clinical trial protocol, including inclusion & exclusion criteria, and accuracy in obtaining any required imaging and pre & post procedural data. Demonstrate proficiency in pre-case planning, CT المزيد...
Clinical Engagement Manager Mea
Partner with local marketing teams to deliver cross-functional commercial and clinical collaboration Manage all clinical activities within the region to generate relevant clinical evidence and medical intelligence, including case studies and QIPs Create content and deliver profess المزيد...
Collaborate with research coordinators, statisticians, clinical/biomedical investigators and other research faculty to implement a statistical analysis plan Develop, write, execute, test, debug, implement, modify and support new or existing statistical or mathematical software prog المزيد...
Create documents for all phases of drug development, including manuscripts, abstracts, posters, oral presentations and slide sets through their lifecycle Independently write first drafts with input from lead author from CSR and/or TFLs Coordinate or complete journal/abstract submi المزيد...
Process regulatory documents per client specifications and rules or according to Synchrogenix standard rulesets and guidances, under agreed timelines, and within agreed quality standards Anonymizing and/or redacting protocols, SAPs, CSRs and other applicable documents in support of المزيد...
. Maintaining and motivating a successful team by recruiting, training, and coaching employees; ensuring a safe, secure, and compliant work environment; providing your team with professional development and growth opportunities. . Within your own statistical programmer team, monitori المزيد...
Principal Regulatory Writer- Clinical Focus
Work closely with client and internal and partner organization teams to lead development of strategies for organizing and preparing regulatory documents Lead a project team, actively participate in development and writing of high-quality documents (study-level and submission level المزيد...
Process regulatory documents per client specifications and rules or according to Synchrogenix standard rulesets and guidances, under agreed timelines, and within agreed quality standards Anonymizing and/or redacting protocols, SAPs, CSRs and other applicable documents in support of المزيد...
جوب هي منصة إلكترونية تربط أصحاب العمل بالباحثين عن عمل من ذوي المهارات، مما يسهل عملية البحث عن فرص العمل وإيجاد أفضل المواهب. أنشئت في عام 2015. و برزت كبوابة الوظائف الرائدة في جميع دول العالم، حيث تجتذب الآلاف من الباحثين عن عمل يوميًا من جميع أنحاء العالم
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