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Job Details

CRA II / Clinical Research Associate Spain

Company: PAREXEL
Location: Madrid
Reference: 08000
Closing Date: 19 Jul 17
Type: Full Time
Salary (£): Competitive
Benefits:

Job Summary:

clinical monitoring

Requirements:

PAREXEL provides monitors with world class technology, training resources, and limited protocol load. You will also be rewarded for your hard work through our CRA bonus incentive program and career advancement opportunities.

Your Key Accountabilities:

Perform all clinical monitoring/site management activities for assigned projects in accordance with PAREXEL's standard operating procedures
Act as PAREXEL's direct contact with assigned clinical sites, and use judgment to assess and ensure overall integrity of study implementation, as well as adherence to study protocol
Conduct qualification visits (QV), site initiation visits (SIV) and monitoring visits (MV) at assigned clinical sites
Good knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Function as a mentor and role model for other CRA team members
Manage clinical monitoring activities, including:

Arranging on-site visits and logistics
Establishment of a site recruitment plan in collaboration with site staff during QV
Monitoring completeness and quality of Regulatory Documentation
Performing site documentation verification
Data collection and drug accountability in accordance with ICH GCP guideline
Monitoring patient safety on-site and addressing any violations in a timely manner

Apply for this job: CRA II / Clinical Research Associate Spain

Contact Information:

Address:  PAREXEL International
The Quays
101-105 Oxford Road
Uxbridge
Middlesex
UB8 1LZ
England
Tel:  +44 1895 238000
Fax:  +44 1895 238494
Website:  Visit Our Web Site
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