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working as an integral part of the pra full-service study team and for a varied mix of sponsors, the Clinical Research Associate is ultimately responsible for the successful management of Investigator sites throughout the trial lifecycle. key .....
pro018841merck & co., inc. kenilworth, n.j., u.s.a. known as merck in the united states and canada, is a Global Health care Leader with a diversified portfolio of prescription medicines, Vaccines and Animal Health products. the difference .....
Clinical research associatelocation: [taiwan] providing innovative solutions for our clients is what we do. but Innovation just for the sake of Innovation isn’t why we do it. side-by-side with our clients, we strive to move drug .....
location: rostock job id_04.18.00.99.05 your responsibilitiesexecution of worldwide Clinical Trial projectsleading all occurring activities of Clinical Trial projects to ensure Compliance with protocols, clinical objectives and regulatory .....
at pra we’re optimistic that, individually and collectively, we can help make tomorrow better than today. we believe that it is our obligation as a company to help our people find meaningful ways to respond to the needs of others around the .....
who are you?you are a forward thinker. you are an innovator that refuses to settle. you want to push the boundaries and change not just what it means to be a Clinical Research Associate, you want to change the future.  you want to learn from .....
who are you?you are a forward thinker. you are an innovator that refuses to settle. you want to push the boundaries and change not just what it means to be a Clinical Research Associate, you want to change the future.  you want to learn from .....
as a top five CRO, we have worked on 100+ marketed drugs across several Therapeutic Areas and conducted the pivotal or supportive trials that led to FDA and/or international regulatory approval of 45+ such drugs.pra Health Sciences wuhan, nanjing, .....
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 Clinical Research Associate (CRA) 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 termination .....
1178 jobs

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