Field Issue Investigator - Automotive Coventry, Warwickshire (Midlands) Competitive The Company SPX is a global multi-industry manufacturing leader committed to operational excellence and execution. With operations in over 35...Field Issue Investigator - Automotive Coventry, Warwickshire (Midlands) Competitive The Company SPX is a global multi-industry manufacturing le ....click title for more details.
My client a leading Biopharmaceutical Company is urgently seeking an Investigator Studies Programme Administrator for a 3 month contract. For a confidential consultation call Robert Wasterfall on 0044 (0) 207 255 6665 or email your CV to robert.wasterfall@secpharma.comMy client a leading Biopharmaceutical Company is urgently seeking a Part-time Investigator Studies Programme Administra ....click title for more details.
My client a leading Biopharmaceutical Company is urgently seeking a Part-time Investigator Studies Programme Administrator for a 4 month contract working 15- 22 hours per week. For a confidential consultation call Robert Wasterfall on 0044 (0) 207 255 6665 or email your CV to robert.wasterfall@secpharma.comMy client a leading Biopharmaceutical Company is urgently seeking a Part-time In ....click title for more details.
Our client is an established CRO operating on a global scale with many offices acrosds Europe. Having an established client base, they offer pioneering digital technologies as a way of operating therefore offering a unique level of service within clinical trials and drug safety. They now seek a CRA to not ony monitor but also be involved in ethic committee submissionsClinical Research Associa ....click title for more details.
Fantastic opportunity to join one of the best and leading CROs in the world. After securing their pipeline with top Pharmaceutical Companies they are now investing in their permanent employees. If you are looking for an improvement, opportunity for growth and development contact us immediately. Duties Act as the main line of communication between the sponsor and the investigator Locating an ....click title for more details.
Fantastic opportunity to join one of the best and leading CROs in the world. After securing their pipeline with top Pharmaceutical Companies they are now investing in their permanent members employees If you are looking for an improvement, opportunity for growth, both life and work balance - contact us immediately. Job Duties Act as the main line of communication between the sponsor and the ....click title for more details.
A varied role for an experienced complaints handlerCOMPLAINTS INVESTIGATOR / COMPLAINTS HANDLER £20-£25,000 pa doeIn order to comply with the financial services dispute resolution rules, all firms are required to have an effective procedure in place for dealing with complaints. Due to a retirement, we now have an opportunity with a leading mortgage services provider to join ....click title for more details.
A varied role for an experienced complaints handlerCOMPLAINTS INVESTIGATOR / COMPLAINTS HANDLER £20-£25,000 pa doeIn order to comply with the financial services dispute resolution rules, all firms are required to have an effective procedure in place for dealing with complaints. Due to a retirement, we now have an opportunity with a leading mortgage services provider to join ....click title for more details.
We are currently looking for a Spanish CRA 2 or SCRA with extensive previous monitoring experience and knowledgeable in Spanish Regulatory and Ethics requirements to work for a leading UK clinical research organisation. This position is to be field based in Madrid or Barcelona and therefore we are looking for candidates who have previous experience of working homebased for a CRO or pharmaceutic ....click title for more details.
We are currently recruiting a Clinical Research Associate, CRA2, to join a leading CRO. You will have previous experience in the monitoring of clinical research trials in Germany and will be office based in Cologne or field based in Berlin or Munich. Job Summary You will be responsible for the administration and full site responsibility for clinical studies according to SOPs, ICH-GCP and l ....click title for more details.
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