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Job Details

CLINICAL RESEARCH ASSOCIATES / home and office-based in Rome and Milan, Italy / 5K EUR SIGN ON BONUS!

Company: Covance
Location: Italy
Reference: 53365BR
Closing Date: 15 Mar 17
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

With more than 47.000 employees around the globe, LabCorp/COVANCE is one of the world's most comprehensive and Experience d contract research organizations (CROs) and laboratory services provider with a tradition of innovation in the science and processes of drug development.

Requirements:

The work we do at Covance impact the lives of millions of people around the world… so could you too as our next Clinical Research Associate?

We have the ability to offer wealth of services covering all aspects of drug development ranging from non-clinical research services through to post-marketing safety and commercialization services. We are currently the only CRO with this depth of service offerings.

Covance has several CRA opportunities for you in various regions of Italy - this is a great moment to join us - up to EUR 5000 Sign on Bonus!

Locations : Rome (office-based or home based) / Milan(home-based)

Our Clinical divisions currently have several needs for Clinical Research Associates in:

  • CoSource - outsourcing division - this is our exclusive client dedicated model (dedicated to one sponsor).

° CRAs (2 to 4 yrs Experience including oncology) - home-based - Rome and Milan

  • Internal Clinical Operations division

° CRAs (min 2 yr monitoring Experience ) - office-based - Rome/ well communicated centers

  • Early Clinical Development division (ECD)

° CRA (min 2 yrs monitoring Experience , phase I - II a plus) - home-based - Rome or Milan preferred but we are open for other locations as well!

Can you bring your drive to our cutting-edge clinical projects?

We need CRA II (ideally from 2 to 4 yrs exp) who are ready to apply their pre-study, initiation, monitoring and closeout visits expertise, and their deep ICH-GCP and SAE management expertise to bring safe, effective and essential medicines to market sooner.

For some roles, experience monitoring international, phases II-III and trials in oncology is a must.

Your rewards :

  • Up to a EUR 5,000 sign on bonus - limited time only, apply now!
  • The opportunity to pursue further training and an interesting career in an inspiring environment that values achievement, supports a balance between your personal and professional life and allows you to make meaningful contributions
  • Flexible conditions and an attractive remuneration package


Education/Qualifications: 

  • University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
  • - Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements
  • - Thorough knowledge of monitoring procedures
  • Basic understanding of the clinical trial process
  • Good in IT
  • E-CRF Experience 
  • Multitasking/ time mgmt
  • Training skills to train sites
  • Stress resistant
  • Confront constructively to get it done as well keep site
  • Experience Minimum of two (2) years of clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits)
  • Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
  • Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
  • Good planning, organization and problem solving abilities
  • Ability to work with minimal supervision
  • Good communication and interpersonal skills
  • Good analytical and negotiation skills
  • Computer competency
  • Fluent in local office language and in English, both written and verbal
  • Works efficiently and effectively in a matrix environment

 

Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.


Interested candidates have to transmit their personal cv according to the Italian legislative decree n° 196/2003.

Apply for this job: CLINICAL RESEARCH ASSOCIATES / home and office-based in Rome and Milan, Italy  / 5K EUR SIGN ON BONUS!

Contact Information:

Address:  Covance- Warsaw


Poland
Tel: 
Fax: 
Website:  Visit Our Web Site

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