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solvay is an equal opportunity employer. we evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected characteristics. .....
actual job title = Associate Director or senior manager, Clinical database programming ******important: must to have management experience, Statistical programmers or sdtm programmers for this posting****** typical daily work hours = 8am to 5pm .....
                                                  we’re continuously advancing science. could you advance with us?   at ucb we’re passionate about science and that’s what drives us to create a .....
accountable for creating and maintaining client relationships, to secure repeat business with assigned customer(s)/projects/portfolio’s through successful delivery of project timelines and quality data whilst maintaining bid profitability .....
Process Engineer – upstream/downstream the ideal candidate for this role will have had 2-3 years of experience support Drug substance Manufacturing Operations through technical investigations and executing technology transfers / new product .....
ideal candidate:we are looking for someone with Analytical Chemistry working experience in synthetic Molecule space. this role is a largely Laboratory-based position, you will be responsible for driving cutting-edge analytical support and technology .....
•individuals with at least 3+ years' experience in Clinical pharmacology trials (ie bioequivalent, drug-drug-interaction, Food effect, etc) •experience in working with phase 1 Clinical research unit (cru) •experience in managing .....
Analytics Consultant (media)symphony Health solutions, a wholly-owned subsidiary of pra Health sciences, is a leading provider of high-value data, Analytics, technology solutions and actionable insights for Healthcare and Life Sciences .....
designs, plans, and executes biostatistical components of Clinical trials. uses sound Statistical methodology to conduct studies, prepares the Statistical components of protocols, and is responsible for the Statistical components of reports.8 years .....
working as an integral part of the pra full-service study team and for a varied mix of sponsors, the Clinical Research Associate is ultimately responsible for the successful management of Investigator sites throughout the trial lifecycle. key .....
126 jobs

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