TRABAJO STUDY CANCER CLINICAL TRIALS MADRID, MADRID

You will join a dynamic and international team of other european clinical development directors that work as part of the global clinical development (gcd) group...

Implementation of study amendment-and changes in study related processes)... knowledge of clinical trials - knowledge of clinical trial conduct, and skill in applying...

Day to day responsibilities will include: support clinical research studies and maintain a safe study environment according to health and safety policies under the...

Understanding of good clinical practice (gcp) standards... life sciences, clinical research, or a related discipline)... periodically review study files to ensure...

study start up associate ii - icf icon plc is a world-leading healthcare intelligence and clinical research organization...   our study start up associates are integral...

study start up associate i / ii - icf icon plc is a world-leading healthcare intelligence and clinical research organization...   our study start up associates are...

You will work with clinical trials patient and operational data, develop new data solutions and set up risk-based monitoring systems in process improvement department...

Our global clinical operations colleagues within our ppd® clinical research services provide end-to-end support for clinical trials from study start up to monitoring...

Oxon is seeking an enthusiastic epidemiologist with experience in observational study designs, to join our dynamic rwe team... join us in building a diverse and...

We are currently seeking a senior clinical research associate to join our diverse and dynamic team... senior cra - spain, madrid icon plc is a world-leading healthcare...

Advanced knowledge of federal regulations, good clinical practice, and good clinical data management practices... main responsibilities include: collaborate with...

Previous experience in clinical trial regulatory submissions... experience working the pharmaceutical, biotechnology or cro industry and knowledge of clinical trials...

The project manager is responsible for maintaining the proper project documentation and ensuring compliance with sops and regulatory requirements for clinical...

We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery... milestone one partners with research sites...

Good understanding of clinical trial contract management... strong understanding of regulated clinical trial environment and knowledge of drug development process...

Thorough knowledge of ich gcp and relevant regulations for the conduct of clinical trials benefits of working in icon: our success depends on the quality of our...