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Clinical Research Associate

Chiltern


Location:
Home Based
Date:
06/01/2017
2017-06-012017-07-01
Job Type:
Employee
Job Status:
Full Time
Categories:
  • Clinical Operations
Chiltern
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Job Details

Chiltern has a great opportunity for experienced Clinical Research Associates (CRAs) to join our growing clinical operations teams.

 

CRAs are home-based and can be located anywhere in the US. We have opportunities in multiple therapeutic areas.  Experience in any of the following areas is a plus:

 

  • Oncology

  • Liver Disease

  • Gastrointestinal

  • Ophthalmology

 

The CRA is a key member of the Clinical Project Team and is responsible for managing investigator sites for selected studies. Incumbents monitor specified sites to ensure data integrity and compliance with Chiltern International or Client’s SOPs, ICH GCP and or ISO 14155, regulatory requirements and the project protocol. Incumbents are responsible for ensuring that projects are completed on time and within budget.

 

Chiltern’s culture is one that offers a great work/home life balance and a competitive benefits package. We are a mid-sized CRO with a large global footprint. If you are looking for a company that offers an environment that encourages growth and advancement reach out to our recruitment team today for more information.

 

Requirements

  • Minimum of 2 years monitoring experience
  • Undergraduate degree, equivalent work experience maybe considered
  • Good attention to detail
  • Good Understanding of ICH GCP and regulatory requirements
  • Good computer literacy with knowledge of PCs, Windows and MS Office applications
  • Experience using clinical trials management systems
  • Good verbal and written communication skills