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[Ci-development] fondly maliciously


From: Tessa Hodge
Subject: [Ci-development] fondly maliciously
Date: Fri, 13 Oct 2006 21:35:01 +0100
User-agent: Thunderbird 1.5.0.7 (Windows/20060909)


Degree: Life science degree expected with particular focus on virology.
Serves as primary contact for the protocol. The candidate will also perform blood processing experiments using microfluidic systems and analyze data. Solids and liquid dosage form experince. Interact with pharmacovigilance units in countries. To intimate any discrepancy in conduct of trial.
Board certified or board eligible is preferred.
Good communication skills.
Field staff Training.
Develops and implements assays to evaluate antiviral drug mechanisms, drug resistance mutations, and analysis of viral isolates at the cellular and molecular level. To fill up CRF on day of recruitment and follow up.
Work with teammates to improve company quality processes.
Knowledge of carrying out, prior art search using databases and Infringement analysis.
Apply results to bug tracking system. A HO licence is preferred.
Apply results to bug tracking system.
A HO licence is preferred. To work in accordance to GLP. Interact with development team to clarify and resolve outstanding issues. This position will be responsible for production of analysis datasets and specifications, well documented code, summary tables and some statistical analysis of data.
Ability to read a lot of material and condense the information.
Ensure that the global pharmacovigilance database is updated periodically. Interact with bug tracking system to monitor fixes and retests. Interact with bug tracking system to monitor fixes and retests.
Provide pharmacovigilance input on designated products. This position will be responsible for production of analysis datasets and specifications, well documented code, summary tables and some statistical analysis of data.
Board certified or board eligible is preferred.
Work with teammates to improve company quality processes. Interact with bug tracking system to monitor fixes and retests.
Participate in company core data sheets and product label changes and medical interpretation of safety data for regulatory documents. Experience in sterile cell culture procedures, cell processing is needed. Knowledge of carrying out, prior art search using databases and Infringement analysis.
Effectively leads a global team of individuals assigned to the protocol.
Perform black-box, guerilla, and regression testing of software products as required. Provide medical assessments of clinical trial and spontaneous event reports. Monitoring of Adverse Events from clinical trials. The candidate will also perform blood processing experiments using microfluidic systems and analyze data. Prepare reports of PMS studies for regulatory submission.
Solids and liquid dosage form experince.


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