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Job Details

Clinical Research Associate - Start-up Team, Madrid or Barcelona-147619

Company: PPD
Location: Europe, Middle East & Africa-Spain-Community of Ma
Reference: 147619
Closing Date: 18 Oct 18
Type: Full Time
Salary (£): On Application
Benefits:

Job Summary:

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. ...

Requirements:

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.


If you are interested in becoming part of PPD Site Intelligence and Activation (SIA) global structure and:
- You have been actively involved in applying and fine-tuning a new start-up model, 
- You have monitoring experience and want to use that experience to help selecting high performing sites, 
- You are looking to build some specific expertise in what is a very important aspect of clinical research; 

Then you might be interested in the role of a: 

Clinical Research Associate - SIA, Madrid


The start-up is a very exciting but challenging period in the life-cycle of a clinical trial. Getting sites quickly and efficiently to the point where they can enroll subjects is crucial to the overall timelines of a study.

As a SIA CRA, you will work on newly awarded projects. You are the initial contact with the site and you will conduct feasibility activities on a country level.
You will evaluate the site and bring it to the point where it is formally selected - or rejected. Your assessment will play a key role in the selection of appropriately qualified sites, thus contributing to the achievement of project operational goals and impacting on the success and profitability of the projects. 

You will work closely with the Contract Specialists and the Country Approval Specialist, under the supervision of the SIA Country Manager, and your shared goal will be to bring investigational sites to the point of initiation and enrollment timely and efficiently.


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Qualifications

In order to be successful on this role you should have:

- University level of education in a life sciences field
- Clinical Monitoring experience is a must
- In-depth knowledge of ICH-GCP, EU and FDA requirements
- Willingness & ability to travel
- Excellent communication and team work skills – in order to establish good communication line between PPD and the site
- Flexibility and ability to work on multiple projects and to support tasks such as feasibilities, site contracts and budgets, submission documentation and contribute to regulatory country intelligence as required
- Experience of starting up clinical studies or contributing to start up tasks.

Knowledge, Skills and Abilities:
  • Proven clinical monitoring skills
  • Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
  • Demonstrated ability to attain and maintain a working knowledge of Good Clinical Practices and applicable Standard Operating Procedures
  • Good oral and written communication skills, with the ability to communicate effectively with medical personnel
  • Customer focus
  • Good organizational and time management skills
  • Effective interpersonal skills
  • Attention to detail
  • Proven flexibility and adaptability
  • 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
  • Good English language and grammar skills
  • Good presentation skills
PPD is an Equal Opportunity Employer
How to apply:
Please submit your CV in English. Only short-listed candidates will be contacted.

Apply for this job: Clinical Research Associate - Start-up Team, Madrid or Barcelona-147619

Contact Information:

Address:  PPD Cambridge
Granta Park
Great Abington
Cambridge

CB21 6GQ
England
Website:  Visit Our Web Site

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