TRABAJO CLINICAL STUDY MANAGER CIUDAD DE MÉXICO, CIUDAD DE MÉXICO

•    responsible for development and ongoing maintenance of clinical study tools and templates, including the clinical monitoring plan... •    demonstrates understanding...

•    responsible for development and ongoing maintenance of clinical study tools and templates,  including the clinical monitoring plan... •    demonstrates understanding...

•    responsible for study management components of inspection readiness for all aspects of the study conduct...   •    clinical research organization (cro) and...

Company description psi is a leading contract research organization with more than 25 years in the industry, offering a perfect balance between stability and innovation...

We focus on delivering quality and on-time services across a variety of therapeutic indications... company description psi is a leading contract research organization...

clinical data programmer icon plc is a world-leading healthcare intelligence and clinical research organization... clinical data programmer location: mexico city...

• 3+ years of clinical research experiences as a: clinical trial assistant or study coordinator... • may lead cta study teams... • knowledge of applicable clinical...

What you will be doing: efficiently drive study initiation: review and negotiate clinical site investigator contracts and budgets... serve as the internal consultant...

clinical system lead - mexico/colombia icon plc is a world-leading healthcare intelligence and clinical research organization... we have an incredible opportunity...

The role: as clinical associate you would be an integral part of the study team whilst acquiring clinical and corporate knowledge of clinical trial conduct...

• performs study duties in adherence to the protocol, clinical management plan (cmp), study processes, ich-gcp and any other requirements stipulated on the...

We are currently seeking a clinical trial manager to join our diverse and dynamic team... clinical trial manager, oncology - latam / remote icon plc is a world-leading...

Supporting study teams in the development of study documents, including protocols, informed consent forms, and investigator brochures... participating in study start-up...

Conduct periodic reviews of study files for completeness... track and manage case report forms (crfs), queries, and clinical data flow... we create intelligent connections...

Brand manager     your tasks & responsibilities:   • assure launch readiness with key metrics on time • expand the testing network for precision medicine and grant...

Iss ssa when working at study sites: • at study sites works with site team to support studies, administratively, to be initiated, conducted and/or completed...

Supporting study teams in the development of study documents, including protocols, informed consent forms, and investigator brochures... previous experience in clinical...