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descriptionthe senior Clinical Research Associate (srcra) is part of Clinical monitoring within tfs develop and will function operationally as a Member of a project team and is responsible for the initiation, on-site and remote monitoring and .....
the Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure Clinical trials are conducted, recorded, and reported in accordance with the science)" rel="nofollow">Protocol, standard operating procedures .....
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 .....
we believe that our people are the future of the industry. we provide a culture in which our employees can enjoy personal satisfaction, professional achievement and have the ability to strategically map out long-term Career plans. if you're ready to .....
    position summary the Associate Director, Clinical project lead is responsible to lead the cross-functional Clinical sub-teams to define study specifications, achieve study milestones through operational feasibility and budget and timeline .....
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 .....
profileeducation: degree in Medicine; post-graduate diploma in one out of the most relevant therapeutic area of our r&d, namely oncology, pain & Inflammation, gastro-enterology. language: fluent in English previous experience: at .....
i: job information:job title: Clinical project leaderfunction: clinicaltype of position: exemptreports to: therapeutic area Director (assistant Director)dept. name: north america Clinical study unit (na, csu)location: bridgewaterii. job summary: the .....
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 application .....
descriptiontfs is a global CRO headquartered in sweden. we genuinely believe that “global in mind and local at heart” is the core of our success. at tfs, you will be offered the possibility to develop in a global organization with a company .....
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