Clinical Research Associate

Two fantastic opportunities have arisin for experienced CRAs to join a globally renowned Pharmaceutical company. There are two contract opportunities one is looking for someone to start as soon as possible and the other is looking for someone with Phase I experience - ideally to start in October. You should be based within easy access of Berkshire to be within easy access of the office. You must know the UK Ethics system thoroughly as they will be actively involved in setting up new UK trials.

You will be accountable for all site management and monitoring activities for clinical trials performed by the company, fostering effective relationships with sites to ensure delivery of the study within planned timelines and according to required standards of quality and compliance.

Home Based

Responsiblities:

*Identify investigatory, perform feasibilty and acess sites with regard to protocol and local requirements.

*Manage assigned investigational trial sites

*Assist in the implementation of recruitment strategies.

*Conduct site visits and prepare monitoring reports in phase I through IV trials in accordance with company SOPs.

*Ensure adequate reporting/tracking of subject site status, protocol deviations and adverse events.

*Assist with and/or prepare all necessary documentation fo regulatory submissions.

*Partner with Clinical Project Management on other aspects of the clinical trials.

Requirements

* BSc or equivelant
*Strong amount of monitoring experience
*Project Management and/or study coordinator experience is preferred
*Previous experience at an investigative site, as a trainer and/or in data management is helpful

KEY WORDS: CRA Clinical Research Associate SCRA Site Manager South East Berkshire London