LAVORO CLINICAL STUDY COORDINATOR

The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety...

Minimum of two years practical experience working as a clinical research coordinator... planning and coordinating logistical activity for study procedures according...

study coordinator, assistente di ricerca, infermiere, medici ricercatori; •buona conoscenza dei protocolli clinici, delle good clinical practice (gcp) e degli aspetti...

study coordinator unità di reumatologia traslazionale                                                                                       il gruppo humanitas,...

Gra, etc) and external key opinion leader/ investigator    management of the interaction with external cro and consultants to support the clinical pharmacology...

Work closely with global study leaders to provide appropriate strategic oversight of a program of studies on behalf of sr gpd and clinical program team (cpt) provide...

clinical section of the investigator’s brochure, protocols and clinical study reports)...   main responsibilities     enhances clinical study execution, working...

clinical section of the investigator’s brochure, protocols and clinical study reports)...   main responsibilities     provide medical and scientific input into clinical...

Provide clinical leadership within the core team, ensuring the clinical perspective informs key strategic decisions...     lead the clinical team in designing...

Provide clinical leadership within the core team, ensuring the clinical perspective informs key strategic decisions...    lead the clinical team in designing...

study documents managed through edms) and supports the cpm in ensuring the compliance of the clinical trial with internal sops and applicable regulations - prepare...

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

Defines clinical supply parameters for irt set up and initiates subsequent updates throughout the duration of the clinical trial... develops, maintains, and executes...

With global clinical research locations all over the world opis offers a full range of integrated clinical research services as scientific advice medical writing...

• gain experience in study procedures by working with experienced clinical staff... • at least 1 year prior clinical experience preferred... ","applicantlocationrequirements":[{"@type":"country"...

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

Leads gcsc group initiatives including the active participation of the study oversight process for gcsc activities to support takeda’s clinical trial operating model...

Collaborate closely with cras and the local study team to achieve study milestones efficiently... • actively participate in local study team (lst) meetings...

Your commitment to quality and compliance will ensure successful study delivery... you will manage study supplies, perform monitoring visits, and prepare for audits...

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