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Clinical trials assistant

Sar*** ***** (XX anos)
Life Sciences Research em Parque de Investigación Biomédica de Barcelona, Spain
Faculty of Medicine, University of Lisbon, Portugal
Almada,
Setúbal
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Experiência
Life Sciences Research
Parque de Investigación Biomédica de Barcelona, Spain
jan 2018 - abr 2018 
Duties and responsibilities: Development and production of biotherapeutics (Chemical synthesis, HPLC and MS techniques); review and update relevant drug information; participate in the administrative and logistic tasks; weekly reports and protocols elaboration; data analysis and graphs elaboration; oral presentations for Life Sciences experts; successful working in a multicultural and multidisciplinary team.
Life Sciences Research
Instituto de Medicina Molecular de Lisboa, Portugal
set 2015 - dez 2017 
Duties and responsibilities: Development of selective-drugs for Alzheimer’s diseases; oral presentations for Life Sciences experts; elaboration of fully detailed reports; develop of new improved processes and perform implementation; meetings organization; orders management, office material storage supply, check and stock control; work-orientation of one medical student; participation in two international conferences.
Formação
Neurosciences
Faculty of Medicine, University of Lisbon, Portugal
out 2014 - jan 2017 
(Grade of 18 values out of 20)
Biochemistry
Faculty of Sciences, University of Lisbon, Portugal
set 2011 - jul 2014 
(Grade of 14 values out of 20)
Idiomas
Portuguese - Advanced
English - Advanced
Spanish - Basic
Informações Adicionais
Key skills and competencies:
 Dynamic and proactive person.
 Ability to plan, organize, prioritize, and execute multiple tasks within assigned objectives.
 Successful working in a team environment, as well as independently.
 Ability to work under pressure and troubleshooting skills.
 Strong attention to detail.
 Good project management skills.
 Willingness and ability to travel.
 Advanced user of MS Office tools (Word, Excel, PowerPoint) and the ability to learn appropriate software.
 Knowledge of data analysis, graphs interpretation and statistic.  Knowledge in GCP, SOPs, CRF completion and submission process for Clinical Trials.  Proven flexibility and adaptability.  Effective oral and written communication skills, with the ability to communicate effectively with medical personnel.
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