TRABAJO CENTRAL MONITORING ASSOCIATE SPONSOR

Or perhaps you are looking a future beyond monitoring with our development opportunities... the role: responsibilities perform site selection, initiation, monitoring...

Senior clinical research associate iqvia is the human data science company oriented to drive human health outcomes forward... your responsibilities will include:...

Broad protocol knowledge, therapeutic knowledge desired... we create intelligent connections to accelerate the development and commercialization of innovative medical...

Compliance monitoring visit (cmv)... fully documents trial related activities, in particular monitoring... 1-2 years of clinical trial monitoring experience is preferred...

• monitoring experience is recommended, or other relevant experience should be considered, such as data management or central monitoring... • create and update trial-specific...

Years of clinical trial monitoring experience is preferred... a minimum of 1 year of clinical trial monitoring experience is required...

central laboratories, ixrs, epro, etc... the global study associate director (gsad) is responsible for the delivery of clinical studies, including quality, timelines...

Mandated as a central resource of the united nations, unops provides sustainable project management, procurement and infrastructure services to a wide range of governments...

Clinical research associate iqvia spain is looking for talented and motivated team member to join our sponsor dedicated team as junior cra...

Compliance monitoring visit (cmv)... fully documents trial related activities, in particular monitoring... may be required to oversee audit and inspection preparation...

Experience: 2+ years of monitoring experience with strong focus on oncology... as a clinical research associate you will be responsible for monitoring clinical trials...

We are currently seeking a senior clinical research associate to join our diverse and dynamic team... what you will be doing: working independently and actively...

As the cra you are the main sponsor representative, providing key project updates... as a clinical research associate (cra) you will coordinate all aspects of the...

Work with our central support office to submit cyber grants on behalf of cpss promote compliance with established sponsor's finance policies, standards and processes...

As the cra you are the main sponsor representative, providing key project updates... minimum 2 years of monitoring and site management experience scientific background...

associate cloud engineer or professional cloud architect or professional data engineer desirable   what's in it for you your strengths and experience count at vodafone...