Clinical Research Associate, sponsor dedicated
... site close-out visits. Perform investigator site management activities in adherence ... guidance to study coordinators and investigators as necessary and in agreement ...
... site close-out visits. Perform investigator site management activities in adherence ... guidance to study coordinators and investigators as necessary and in agreement ...
... Analysis and Data Management Plan, Investigator Brochure, medical input to the ... of Development, Proof of Clinical Principle, Release of Full Development, Release ... Clinical Development, you: You author Investigator`s Brochures, Asset Evidence Plans, Core ...
... Analysis and Data Management Plan, Investigator Brochure, medical input to the ... of Development, Proof of Clinical Principle, Release of Full Development, Release ... Clinical Development, you: You author Investigator`s Brochures, Asset Evidence Plans, Core ...
... , and maintain strong relationships with investigators staff that will ensure high ... the study. Interact train new investigators to work on the client ... to have scientific discussions with Investigators and Site Personnel BA BS ...
... will coordinate with institutions and investigators at the local level. A ... Trial Master File (eTMF), electronic Investigator Site File (eISF) (Florence) We ...
... and advance, be a curious investigator and problem solver Experience with ...
... to Regulatory Authorities Ø Interfaces with Investigators, external service providers and CRAs ...
... the trial process. Collaborating with investigators and site staff to facilitate ...
... clinical activities Participate in Sponsor, Investigator and bid defense meetings Lead ...
... in klinischen Studien als sub-investigator (GCP-Training)Qualifikation zu DKG ...