Location: Office or Home Based Anywhere in Spain
Closing Date: 06 Nov 16
Type: Full Time
Salary (£): On Application
Chiltern is Europe’s largest privately owned Clinical Research Organization, with over 4200 employees and 47 offices throughout Europe, both Eastern and Western, North America and in Asia. We have worked in virtually every therapeutic area for all the major pharmaceutical companies and very many of the smaller ones. The Chiltern Source department currently looking for a SRCRA to work for the client, homebased or Chiltern Office.
To prepare and conduct all site visits including, but not limited to, qualification visits, initiation visits, monitoring visits, motivational visits, audit support visits, and termination visits in accordance with study monitoring plan and client’s SOPs.
Develop and maintain good working relationships with assigned study sites in order to effectively manage each site through the clinical trial and be proactive in dealing with any issues, e.g. recruitment
Document all site visits within visit reports in a timely manner.
Appropriate follow-up with sites after monitoring visits to document findings and resolution of identified issues.
Be an integral team member and support the study team to ensure the smooth-running of the clinical trial.
Update all Client Clinical Trial Systems as required to provide effective study status updates for assigned sites
At least with 3 years working experience in a similar position at pharmaceutical company or CRO
Health care or Health Sciences graduate
Experience in performing all visits types: SQV, SIV, SMV, and COV
Experience across a number of phases and therapeutic areas
Knowledge and experience of Regulatory and Ethics Committees submissions.
Competence using electronic systems e.g. CTMS, eCRF
Basic IT competence required (email, internet, word, excel)
Good standard of oral and written English
Centro Empresarial, Euronova, 3 Ronda de Poniente, 0,2Âº, 28760 Tres Cantos, Madrid, Spain
|Tel:||+34 91 187 27 00|
|Fax:||+34 91 187 28 49|
|Website:||Visit Our Web Site|
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