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celerion is looking for a Clinical Project Manager in our Clinical Project Management group to be responsible for the independent operational and financial management and oversight of multi-center and/or external Clinical site activities, .....
job description at quintiles we help Healthcare and biopharma companies improve their probability of success. we do this by connecting our scientific, therapeutic and Analytics expertise with superior delivery. from advisory through Operations, .....
job description at quintiles we help Healthcare and biopharma companies improve their probability of success. we do this by connecting our scientific, therapeutic and Analytics expertise with superior delivery. from advisory through Operations, .....
the lead Clinical Trial operations manager (lead ctom) is responsible for all operational aspects of Clinical Trial oversight including the delivery of every study on time within budget and scope in Compliance with gcp’s, sops and standards.the .....
at abbott, we're committed to helping people live their best possible life through the power of Health. for more than 125 years, we've brought new products and technologies to the world -- in Nutrition, Diagnostics, Medical Devices and branded .....
the lead Clinical Trial operations manager (lead ctom) is responsible for all operational aspects of Clinical Trial oversight including the delivery of every study on time within budget and scope in Compliance with gcp’s, sops and standards.the .....
job description join us on our exciting journey! iqvia™ is the human Data Science company™, focused on using data and science to help Healthcare clients find better solutions for their patients. formed through the merger of ims Health and .....
descriptionthe Project Manager has the overall responsibility for managing projects in accordance with company policies, sops, regulatory requirements in addition to financial and contractual obligations. the Project Manager will plan and .....
responsibilities essential function:conduct and facilitate specific start-up activities such as feasibility, site identification, pre- Qualification, site regulatory package (srp) review and approval, Informed Consent (icf) customization, irb/iec .....
do you want to watch Clinical Development change, or do you want to be the one to shape it? because we’re hoping you’re here for the latter. who are we?we are pra Health Sciences. we provide innovative Drug Development .....
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