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Job Details

Clinical Research Associate - Netherlands-131933

Company: PPD
Location: Europe, Middle East & Africa-Netherlands-Gelderlan
Reference: 131933
Closing Date: 07 Dec 16
Type: Full Time
Salary (£): On Application
Benefits:

Job Summary:

PPD is currently recruiting for CRA's to join the Clinical Management team in Bennekom.The Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and PPD Standard Operating Procedures.   Conducts site visits to assess protocol and regulatory compliance and manages required documentation. ...

Requirements:

PPD is currently recruiting for CRA's to join the Clinical Management team in Bennekom.

The Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and PPD Standard Operating Procedures.   Conducts site visits to assess protocol and regulatory compliance and manages required documentation. Responsible for ensuring that data will pass international quality assurance audits. Represents PPD in the global medical research community and develops and maintains collaborative relationships with investigational sites and client company personnel.   Will assist project manager or clinical team manager on assigned projects and will take a lead role where required. Will support the line manager to mentor, train and contribute to the development of junior clinical team members. Required to travel 60-80% on average.   IndeedPPDEMEA1

Qualifications

  Education and Experience:
  • University degree in a science related field or a certified health care professional or equivalent certification/licensure from an appropriately accredited institution 
  • Considerable clinical research monitoring experience (comparable to 5 years) with a demonstrated high level of expertise in all aspects of clinical monitoring
  • Fluency in English and in the country's native language
  • Valid Driver's License where applicable
  • In some cases an equivalent combination of education, professional training, and experience that provides the required Knowledge, Skills and Abilities may be considered
  Knowledge, Skills and Abilities:
  • Expert clinical monitoring skills
  • Expert knowledge of FDA guidelines, GCPs and applicable Standard Operating Procedures
  • Skills to mentor and train other monitors in a positive and effective manner
  • Demonstrated ability to evaluate medical research data and proficient knowledge of medical terminology
  • Excellent oral and written communication skills
  • Strong customer focus
  • Excellent interpersonal skills
  • Excellent organizational and time management skills
  • Strong attention to detail
  • Proven flexibility and adaptability
  • Excellent team player with team building skills
  • Effective presentation skills
  • Ability to work independently as required
  • Ability to utilize problem-solving techniques applicable to constantly changing environment
  • Good computer skills: good knowledge of Microsoft Office and the ability to learn appropriate software
  • Good English language and grammar skills
PPD is an Equal Opportunity Employer


Apply for this job: Clinical Research Associate - Netherlands-131933

Contact Information:

Address:  PPD Cambridge
Granta Park
Great Abington
Cambridge

CB21 6GQ
England
Tel:  +44 1223 374100
Website:  Visit Our Web Site

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