TRABAJO CLINICAL TRIALS

Ensures site staff have current gcp and necessary protocol, compound and systems training to conduct the clinical trial... ensures clinical drug supplies are...

Optimize clinical trial supply chain strategies for efficiency and cost-effectiveness aligning with customer requirements... this senior-level position requires...

Prepares and/or reviews regulatory documents to support clinical trial submissions... independently provides regulatory support for complex projects and programs...

Prepares and/or reviews regulatory documents to support clinical trial submissions... prepares and maintains core clinical trial submission dossiers in accordance...

Training / strong knowledge on good clinical practices... extensive knowledge of all steps included in a clinical trial... experience: 2-3 years of experience in...

You will review external vendor quotations maintain vendor databases and tracking systems support vendor identification, assessment activities, vendor selection...

You willreview external vendor quotationsmaintain vendor databases and tracking systemssupport vendor identification, assessment activities, vendor selection and...

These services ensure our clinical research activities are of the highest quality... #li-dariashv iqvia is a leading global provider of advanced analytics, technology...

Experience (years/area): at least 2 years in negotiation with the vendors necessary to carry out clinical trials, in cro or sponsor... negotiate and optimize purchasing...

Me interesa me interesa política de privacidad... horario: jornada completa salario: a convenir... descripción de la empresa empresa multinacional de servicios...

Knowledge of good clinical practices and regulatory requirements for the conduct of high-quality oncology clinical trials is required...  learn more at https://www...

•    leads/chairs the strategic clinical teams... •    provides clinical/medical guidance to the clinical study teams to ensure alignment of clinical trials conduct...

clinical input to nda/bla)... prepare and provide input to clinical study reports (csrs) and clinical portions of regulatory documents (e...

Additional responsibilities include management of clinical trials approvals with local irbs and/or competent authorities... they are looking for a clinical affairs...

Facilitate communication between clinical sites and other abbott clinical staff (e... maintain and develop a productive clinical territory: develop and maintain...

The director, clinical project scientist (cps) develops and leads goals/objectives and end to end delivery of clinical trials within the oncology therapeutic area...

The clinical project scientist (cps) works in the oncology global medical affairs group and will actively participate and may lead aspects of the development, oversight...

Reports the status of clinical trials to management...   early clinical development and clinical pharmacology experience is preferred...   regularly surveils/assesses...