TRABAJO INITIATION CLINICAL ASSOCIATE STUDY

Provides matrix management of functional area representatives to cross functional clinical study teams... the associate director study leader, early oncology clinical...

Serve as the medical expert for clinical study team... this is what you will do: the associate medical director provides input into a clinical study protocol and...

Good understanding of clinical study management including monitoring, study drug handling and data management... manages study supplies (isf, etc), drug supplies...

We are currently seeking an associate director, clinical project scientist (oncology)... the clinical project scientist (cps) works in the oncology therapeutic area...

The clinical scientist will collaborate with study responsible physician(s) in monitoring of clinical trial conduct... the clinical scientist provides input to the...

Abiomed, part of johnson & johnson's medtech, is recruiting for a clinical research associate ii... our team focuses on future development of the impella platform...

Typical accountabilities • provides operational expertise to the study team... • drive risk management and quality efforts to ensure study compliance...

clinical research associate (sr... monitor activities at clinical study sites to assure adherence to gcp, ich, sops, and study protocols...

Assist in developing crf specifications from the clinical study protocol and coordinate the review/feedback from all stakeholdersassist in building clinical databases...

Arranges for the appropriate destruction of clinical supplies... a minimum of 2 years of clinical trial monitoring experience is required...

Follow us on linkedin to learn more about your future with george clinical... what are our expectations of candidates?bachelor degree in a science or related field...

You will be responsible for the identification, definition and delivery of improvements in end-to-end clinical study delivery, utilising tools and techniques to...

Arranges for the appropriate destruction of clinical supplies... ensures site study supplies (such as non-investigational product (ip), lab kits, etc...

study files, crfs, etc... study files, crf files, monitoring files, etc... log in, tracking, quality control as appropriate for the study   • *to share responsibility...

study start up associate / contract specialist at icon, it’s our people that set us apart... study start up associate ii as a member of the study start up team,...

study start up associate / contract specialist at icon, it’s our people that set us apart... study start up associate ii as a member of the study start up team...

study start up associate ii as a member of the study start up team, you will play an integral role in making sure that physicians at our research sites are prepared...

Icon plc is a world-leading healthcare intelligence and clinical research organisation... the role: • to review and negotiate clinical site investigator contracts...

As an experienced clinical research associate, you could be looking to broaden your therapeutic, geographic or study exposure... join us in our exciting journey!!...