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Clinical Research Associate - Italy (m/w/d) (DE)

Aristo Personnel [9662]
Clinical, Clinical Research Associate (CRA), Pharma, Top 100 CISA

! Kunde ist informiert, dass ich die region nicht betreue Streue es allerdings einfach mal in Abstimmung mit ihm in meinem Netzwerk To support our Clinical Operations Team we are looking for a field-based Clinical Research Associate (CRA) – home-based in Italy Preferentially located in Milan or Rome   Your tasks: Monitoring of sites participating in national and international clinical studies according to ICH-GCP, applicable ISO standards and legal regulations. You will be involved in all phases of the study (site selection, site set up, conduction & site closure) Support of the project management team in the coordination of studies and set up of study documents according to national requirements Support in preparation and submissions to Ethics Committees and Regulatory Authorities Your Profile: A degree in life science or a medical education At least 1 year experience in conducting clinical studies Authorization to work as CRA in Italy (as required by M.D. 15Nov2011) Profound command of English in speaking and writing Excellent communication skills as well as ability to complete tasks in an accurate, flexible and timely manner Willingness to travel up to 70 % of your working hours We offer: A professional, international team with high priority of collegiality and team spirit Field-based location in your home office in Italy Regular trips to the Headquarter in Mannheim for face-to-face meetings with the team A company with focus on work/life balance Flexible working hours, full-time as well as part-time possible

! Kunde ist informiert, dass ich die region nicht betreue

Streue es allerdings einfach mal in Abstimmung mit ihm in meinem Netzwerk

 

 

To support our Clinical Operations Team we are looking for a field-based

Clinical Research Associate (CRA) – home-based in Italy

Preferentially located in Milan or Rome

 

Your tasks:

      • Monitoring of sites participating in national and international clinical studies according to ICH-GCP, applicable ISO standards and legal regulations. You will be involved in all phases of the study (site selection, site set up, conduction & site closure)

      • Support of the project management team in the coordination of studies and set up of study documents according to national requirements

      • Support in preparation and submissions to Ethics Committees and Regulatory Authorities


Your Profile:

      • A degree in life science or a medical education

      • At least 1 year experience in conducting clinical studies

      • Authorization to work as CRA in Italy (as required by M.D. 15Nov2011)

      • Profound command of English in speaking and writing

      • Excellent communication skills as well as ability to complete tasks in an accurate, flexible and timely manner

      • Willingness to travel up to 70 % of your working hours

 

We offer:

      • A professional, international team with high priority of collegiality and team spirit

      • Field-based location in your home office in Italy

      • Regular trips to the Headquarter in Mannheim for face-to-face meetings with the team

      • A company with focus on work/life balance

      • Flexible working hours, full-time as well as part-time possible

map Italy, date_range asap update Permanent
Direct contact

Christina Serafim

Associate Senior Consultant
mail c.serafim@aristo-group.com
phone +49 89 599 1827 200


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