... will be doing: You will monitor multiple Phase I, II, III & IV clinical trial sites, across different therapeutic areas. ... are key to successful trial conduct. As the CRA you ... experience in the pharma or clinical research industry. Minimum 3 years ...
... will be doing: You will monitor multiple Phase I, II, III & IV clinical trial sites, across different therapeutic areas. ... are key to successful trial conduct. As the CRA you ... experience in the pharma or clinical research industry. Minimum 3 years ...
... will be doing: You will monitor multiple Phase I, II, III & IV clinical trial sites, across different therapeutic areas. ... are key to successful trial conduct. As the CRA you ... experience in the pharma or clinical research industry. Minimum 3 years ...
... Consulting projects.Relevant experience in clinical trial data optimization, clinical data management, MAA submissionsRegulatory Intelligence – Pharmacovigilance, Clinical Trial, New and post approval registrations, ...
... role provides a bridge between Clinical Development, Medical Affairs and the ... as well as those in clinical development.Duties and Responsibilities·Builds ... in development and implementation of clinical trials.·Experience of working in a ...
... guidance for optimal conduct of clinical trials, regulatory agency meetings, orphan designations, ... regulatory positions and strategyKnowledgeable of clinical trials methodology, including a working knowledge ...
IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting ... of work experience in the clinical trial space or at least two ...
... scientific services spanning clinical trials, real world evidence, ... management, and clinical to execute daily tasks associated with providing clinical data management to the sponsored pharma industry research trials.· Support the project team during ...
... scientific services spanning clinical trials, real world evidence, ... management, and clinical to execute daily tasks associated with providing clinical data management to the sponsored pharma industry research trials.· Support the project team during ...
... data, including experience reviewing pre-clinical and clinical trial data and output from statistical ...