Postdoctoral Position (extended deadline)
- 25 febrero, 2014
- /
- 0
THE ANDALUSIAN PUBLIC FOUNDATION FOR THE BIOMEDICAL RESEARCH IN MALAGA (FIMABIS), LOCATED IN MALAGA, SPAIN, INVITES QUALIFIED EXPERIENCED RESEARCHER TO EXPRESS THEIR INTEREST FOR A POSTDOCTORAL POSITION TO COORDINATE THE UNIT OF CLINICAL RESEARCH AND CLINICAL TRIALS” OF THE BIOMEDICAL RESEARCH INSTITUTE OF MALAGA(IBIMA)
UICEC
Principal investigator: Maria Isabel Lucena.
Center: IBIMA/ Hospital Universitario Virgen de la Victoria
Functions
February, 28th 2014. 15.00 pm. Extended March, 7th 2014. 15.00 pm
Selection process
After the selection of the best CVs, the candidates will be interviewed
Descargar en PDF
co-funded by the European Fund for Regional Development (FEDER)
THE ANDALUSIAN PUBLIC FOUNDATION FOR THE BIOMEDICAL RESEARCH IN MALAGA (FIMABIS), LOCATED IN MALAGA, SPAIN, INVITES QUALIFIED EXPERIENCED RESEARCHER TO EXPRESS THEIR INTEREST FOR A POSTDOCTORAL POSITION TO COORDINATE THE UNIT OF CLINICAL RESEARCH AND CLINICAL TRIALS” OF THE BIOMEDICAL RESEARCH INSTITUTE OF MALAGA(IBIMA)
UICEC
Principal investigator: Maria Isabel Lucena.
Center: IBIMA/ Hospital Universitario Virgen de la Victoria
Functions
February, 28th 2014. 15.00 pm. Extended March, 7th 2014. 15.00 pm
Selection process
After the selection of the best CVs, the candidates will be interviewed
Descargar en PDF
co-funded by the European Fund for Regional Development (FEDER)
- Methodological advice and support to Clinical trials
- Evaluation of Clinical Trials
- Design of Protocols and running of Clinical Trials Phase I & II
- Pharmacovigilance tasks and elaboration of reports
- PhD in Medicine or Pharmacy
- Experience in the Evaluation of Clinical Trials
- Experience in Drug Regulatory Affairs
- Experience in Protocols and Clinical Trials Phase I & II
- Experience in Pharmacovigilance tasks and elaboration of reports
- High level of English (written and spoken)
- At least 3 years relevant research experience
- Must have published paper(s) in quality journals
- Evidence of proactive organisational capabilities
- Ability to assess and organise resources
- Ability to communicate complex information clearly
- Ability to build contacts and participate in internal and external networks and research presentations
- Use of office packages, especially Excel, as well as databases
- Team worker, highly motivated, supportive of colleagues within the group
- Training in Clinical Pharmacology
- Experience in the Development of Clinical Trials
- Experience in Methodological advice and support to Clinical trials
- Experience in Regulatory & GCP in Clinical research
- Full-time Job

- Methodological advice and support to Clinical trials
- Evaluation of Clinical Trials
- Design of Protocols and running of Clinical Trials Phase I & II
- Pharmacovigilance tasks and elaboration of reports
- PhD in Medicine or Pharmacy
- Experience in the Evaluation of Clinical Trials
- Experience in Drug Regulatory Affairs
- Experience in Protocols and Clinical Trials Phase I & II
- Experience in Pharmacovigilance tasks and elaboration of reports
- High level of English (written and spoken)
- At least 3 years relevant research experience
- Must have published paper(s) in quality journals
- Evidence of proactive organisational capabilities
- Ability to assess and organise resources
- Ability to communicate complex information clearly
- Ability to build contacts and participate in internal and external networks and research presentations
- Use of office packages, especially Excel, as well as databases
- Team worker, highly motivated, supportive of colleagues within the group
- Training in Clinical Pharmacology
- Experience in the Development of Clinical Trials
- Experience in Methodological advice and support to Clinical trials
- Experience in Regulatory & GCP in Clinical research
- Full-time Job
