... : As a Cardiology, Physician Clinical Reviewer you will be a ... lives, in a non-clinical environment. You can enjoy better ... : As a Cardiology, Physician Clinical Reviewer you will be a ... lives, in a non-clinical environment. You can enjoy better ...
pl.jooble.org
... term experience in clinical affairs clinical research project management in the ... relevant regulatory requirements for clinical studies and clinical evaluations for medical devices (ICH- ... planning and conducting clinical studies with proven success. Other ...
www.iagora.com
... : As a Cardiology, Physician Clinical Reviewer you will be a ... lives, in a non-clinical environment. You can enjoy better ... : As a Cardiology, Physician Clinical Reviewer you will be a ... lives, in a non-clinical environment. You can enjoy better ...
pl.talent.com
... : As a Oncology, Physician Clinical Reviewer you will be a ... lives, in a non-clinical environment. You can enjoy better ... : As a Oncology, Physician Clinical Reviewer you will be a ... lives, in a non-clinical environment. You can enjoy better ...
pl.talent.com
... will compile, publish and produce Clinical Trial Authorization Applications and associated CTA ... to the regulatory aspects of clinical trials are tracked in the company- ...
www.infopraca.pl
... will compile, publish and produce Clinical Trial Authorization Applications and associated CTA ... to the regulatory aspects of clinical trials are tracked in the company- ...
pl.jooble.org
... in Eastern Europe Responsibilities: Supporting Clinical Trial Transparency deliverables, in cooperation with ... -5 years of experience in Clinical Trial Transparency area Experience and technical skills within Clinical Trial Transparency, as a part of ...
pl.jooble.org
... in Eastern Europe Responsibilities: Supporting Clinical Trial Transparency deliverables, in cooperation with ... -5 years of experience in Clinical Trial Transparency area Experience and technical skills within Clinical Trial Transparency, as a part of ...
pl.talent.com
... will compile, publish and produce Clinical Trial Authorization Applications and associated CTA ... to the regulatory aspects of clinical trials are tracked in the company- ...
pl.talent.com
... relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, Research Assistant, nurse, medical assistant, other medical profession Good knowledge of clinical trials, combined with in-depth knowledge ...
pl.talent.com