The Andalusian Public Foundation for the Biomedical research in Malaga (FIMABIS), located in Malaga, Spain, invites qualified experienced researcher to express their interest for an Early stage position as a clinical research associate and monitor of the Unit of Clinical research and Clinical trials” of the Biomedical Research Institute of Malaga(IBIMA) Project: IDPROYECTO, UICEC IBIMA Investigador Principal: Mª Isabel Lucena Lugar de Realización: Hospital Universitario Virgen de la Victoria Functions

• Methodological advice and support to Clinical trials
• Clinical trial Monitoring
• Evaluation of Clinical Trials
• Design of Protocols and running of Clinical Trials
• Pharmacovigilance tasks and elaboration of reports
• All of them in all sort on independent clinical studies

Evaluation criteria

• Grade in Health Sciences
• Experience in the Evaluation of Clinical Trials, Pharmacovigilance and elaboration of reports
• High level of English (written and spoken)

Desirable criteria

• Training in Clinical Pharmacology
• Experience as clinical researcher and training and expertise in patient management and clinical trial design, follow up and results evaluation
• In-depth understanding of Phase I- IV drug development
• Broad experience in the principles and techniques of data analysis, interpretation and clinical relevance/li>
• At least 3 years relevant clinical & 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
• Dedicated highly motivated scientist with exceptional organizational, problem-solving skills, supportive of colleagues and team work capacity
• Participation in research projects as principal investigator or as a collaborator
• Technology transfer activities: patens, licences, collaboration agreements with enterprises
• Complementarities with strategic research areas of the Institute

How to apply Applications should include a cover letter summarizing the applicant’s career and how it will contribute to make the Clinical Trials Unit more competitive and international (1 page), CV, a list of publications ( with 10 most significant publications in the last five years (2011-2015) indicated), and contact information of two references. Status

Full-time Job

Application details

For one year renewable

Application e-mail: rrhh@ibima.eu, write the reference IDPROEAR1810 in the email subject

DEADLINE: receiving applications until October 25, 2016 at 15:00 .

Process of selection After the selection of the best CVs, the candidates will be interviewed. Scale of assessment

Curriculum vitae

Previous experience in clinical trials

Complementary training

Other achievements related to this position

Personal interview