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Job Details

Clinical Research Associate - Italy-141858

Company: PPD
Location: Europe, Middle East & Africa-Italy-Lombardia-Milan
Reference: 141858
Closing Date: 15 Sep 18
Type: Full Time
Salary (£): On Application
Benefits:

Job Summary:

PPD is recruiting for experienced CRA and Senior CRAs for our growing Italian division. As one of the world's largest CRO's, our CRA's have the opportunity to work on challenging projects across a wide range of therapy areas with some of the most innovative pharmaceutical and biotech companies in the world.   PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. ...

Requirements:

PPD is recruiting for experienced CRA and Senior CRAs for our growing Italian division. As one of the world's largest CRO's, our CRA's have the opportunity to work on challenging projects across a wide range of therapy areas with some of the most innovative pharmaceutical and biotech companies in the world.

 

PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 47 countries and approximately 20,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to help clients and partners bend the cost and time curve of drug development to deliver life-changing therapies that improve health. For more information, visit www.ppdi.com.

  • You should thrive in multi-national project teams and be focused on delivering exemplary levels of customer service on multiple, challenging projects.
  • You will have excellent communication and interpersonal skills and are looking to work in a collegiate environment where you want to take true ownership for your work. 
  • You will perform and coordinate all aspects of the clinical monitoring process. You shall also be qualified to conduct monitoring activities independently.

In return we will offer you a positive and supportive working environment within one of the most engaged teams in the industry; who are truly recognised as the cornerstone of our success. We will provide you with meaningful and challenging work and the opportunity to acquire valuable personal and professional skills; through our best in class training and development. 

Qualifications

Education and Experience:

•    University degree in a life-sciences field
•    Qualified as a CRA as per the Ministerial Decree dated 15/11/2011
•    At least 1.5 years’ monitoring experience in clinical development  
•    Demonstrated understanding of ICH-GCP, EU and FDA requirements
•    Fluency in English and in Italian
•    Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
•    Exceptional communication, organizational and time management skills
•    Ability to work in a team or independently as required
•    Good computer skills: good knowledge of Microsoft Office and the ability to learn appropriate software




HOW TO APPLY:
Please submit your CV in English.
 
Registration on our website will also give you the opportunity to be considered for other positions if this one is not the most appropriate for your qualifications and experience.
 
This is an on-going search. Suitable candidates will be contacted accordingly.

Pharmaceutical Product Development, LLC is firmly committed to Equal Employment Opportunity (EEO) and prohibits employment discrimination for employees and applicants based on age, race, color, pregnancy, gender, gender identity, sexual orientation, national origin, religion, marital status, citizenship, disability or protected veteran or other status protected by federal, state, and/or local law.

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Apply for this job: Clinical Research Associate -  Italy-141858

Contact Information:

Address:  PPD Cambridge
Granta Park
Great Abington
Cambridge

CB21 6GQ
England
Website:  Visit Our Web Site

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