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SCRA

Category	Clinical Research
Job Ref	AL/HQ00007093
Job Type	Permanent
Salary	Salary on application
Location	Bulgaria

01 Mar 2010

This is an excellent opportunity for a an experienced CRA to join a global CRO.

Core Responsibilities

- As a Senior Clinical Research Associate you would also perform trial initiation, close out activities, you would coordinate monitoring activities, manage site activities to ensure clinical data integrity in line with company Regulatory and Ethical guidelines for Good Clinical Practice.
- As Senior CRA you would provide clinical and technical support and would develop CRF's and act as liaison between monitoring and other functions.
- You would also operate as the focus for communication with Clinical Research Associates and the Sponsor. You would also act as the lead contact of the project team with study site personnel and also act as a mentor for CRA's .

-As you would report to the project leader and may assume the role of Lead CRA by providing direction to the project team.

Qualifications and Skills Required

-Experience as a Clinical Research Associate
-Co-ordination skills
-Experienced in conducting allocated tasks
-Maintain up-to-date knowledge of ICH-GCP, EU CT Directive and FDA guidelines

For further information please contact
Alina Lapadatu
Email: alina.lapadatu@hayspharma.com

Services advertised by Hays Pharma are those of an Agency and/or an Employment Business