Paramount Clinical Research: Clinical Research Associate II – CRA – West London
A number of Clinical Research Associates (CRA) are currently being recruited for an international Clinical Research Organisation (CRO) within commuting distance from London. It’s an excellent company to join who provide great training and help with career development whichever direction you want to go in.

The responsibility of a Clinical Research Associate (CRA) is to perform all clinical monitoring / site management activities for assigned clinical projects in accordance with SOPs. A Clinical Research Associate (CRA) is responsible for achieving and maintaining high site performance, managing clinical monitoring activities which include the ownership of investigator sites, the selection of investigator/sites, collating Regulatory Documentation, initiating and monitoring of sites, performing site documentation verification, data collection and drug accountability in accordance with ICH-GCP guidelines. If applicable a Clinical Research Associate (CRA) may also act as a Clinical Lead.
The Clinical Research Associate (CRA) will maintain a positive, results orientated work environment, building partnerships and modeling teamwork, communicating to the team in an open, balanced and objective manner. They perform the role of Clinical Lead as/if required on allocated project, exercising ownership for project activities which are related to the monitoring function. They build and maintain good and effective relationships with sites and prepare and submit or support those involved in regulatory and ethics committee submissions and in the generation of Financial Agreements according to standard and local country practices. Other aspects of the role include initiating investigational sites to ensure that they have a thorough understanding of the clinical protocol and that they understand their obligations to conduct a clinical trial as required by applicable regulations.

To be considered and work as a Clinical Research Associate (CRA) it is essential have previous experience monitoring clinical trials in the UK. A scientific or related qualification is also required with flexibility to travel along with strong communication skills. Experience working in a matrix environment would be a bonus and holding a full driving license is essential.

For a full job description, more details or a confidential discussion call Gareth on 0121 616 5135 or email now.

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