Clinical Research Associate - Start-up - Madrid or Barcelona
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:
- 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.