LAVORO CRA SENIOR CLINICAL

clinical section of the investigator’s brochure, protocols and clinical study reports)...     drive medical and scientific input into clinical trial design and execution...

Req • knowledge of clinical trials - knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i...

We’re looking for a  senior regulatory affairs manager  to lead and support regulatory activities across europe... senior regulatory affairs manager (remote - eu/uk) ...

Requisiti• certificazione (laurea in discipline sanitarie/scientifiche, 40 ore di formazione teorica, 10 visite di monitoraggio, almeno quattro mesi di esperienza...

On behalf of the senior global clinical operations program director (sr gpd), the gpd provides strategic operational leadership and oversight of a suite of global...

Ensure that clinical pathways activities align with regulatory standards and internal policies... experience with pathway modelling tools, health economics software...

clinical expertise demonstrate a deep understanding of clinical science supporting our products in electrophysiology & gather/develop data intelligence in our...

Who we are looking for purpose the clinical project management head is a senior leadership role within the clinical operations function, responsible for the line...

clinical research and program management experience working with clinical programs within medical affairs, clinical research, regulatory, cmc or other drug development...

• superior clinical research operational knowledge... • 6-8 years clinical trial management experience in the pharmaceutical industry or cro...

External collaborators include academic and clinical researchers... understanding of clinical trial design, execution, and regulatory requirements (e...

clinical research associate (sr... cra at allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions...

Solid knowledge of good clinical data practices, gcp and regulatory requirements... minimum 5 years of experience in clinical data management in cros or pharmaceutical...

May directly support clinical operations program leads in day-to-day activities for complex and/or business-critical clinical studies (including providing clinical...

For the following job opportunity: job location: cambridge, ma position: senior manager, programming position description: takeda development center americas, inc...

Develop immunogenicity analytical clinical strategy based on drug candidate's immunogenicity risk assessment... direct bioanalytical activities related to clinical...

As a clinical research associate (cra) in italy, you will be at the forefront of scientific innovation, playing a crucial role in delivering studies at allocated...

Good clinical practice (gcp) and international conference on harmonization (ich) guidelines... iqvia is a leading global provider of clinical research services,...

Good clinical practice (gcp) and international conference on harmonization (ich) guidelines)... good clinical practice (gcp) and international conference on harmonization...