Teva Pharmaceuticals Hiring notification for Clinical Research
Qualifications :- M Pharmacy in Pharmacology or B Pharmacy plus M. Sc. in clinical research
Experience Required – 2 – 4 Years
Date posted – November 10
Location – Mumbai
Regulatory/ethics submission of CT as per timelines and to ensure regulatory documents are available, complete and current.
In coordination with the project manager and/or medical monitor, perform study site selection visits. Participate in/conduct investigator’s meeting and site initiation visits.
To perform regular monitoring visits to site and prepare monitoring reports
To ensure the compliance to ICH-GCP guidelines, local & international regulations (i.e. DCGI, FDA) and applicable SOPs.
To ensure that the clinical trial supplies are appropriately handled and adequately maintained at the site as per the project requirements.
Evaluates the speed of recruitment and propose alternative solutions if the predefined objectives are not met, either in the terms of patient number or timelines.
Conduct site close out and assure appropriate archival of controlled documents.
Maintain contacts outside the regular onsite visits, by appropriate communication means, to regulate or to motivate work to be performed by investigators or their staff. These contacts are always recorded and regularly transmitted to the project manager/project team.
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