Vaga de parceiro

Sr CTA - São Paulo / SP

Disponível para Assinantes
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Detalhes da Vaga

  • Escolaridade Não Informado
  • Segmento Não Informado
  • Salário Não Informado
  • Área de AtuaçãoDiversos / Outros

O que você irá fazer

  • Essential FunctionsAssist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) teams with updating and maintaining clinical documents and systems (e.
  • g.
  • , Trial Master File) to track site compliance and performance within project timelines.
  • Collaborate with the clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
  • Assist with periodic review of study files for completeness.
  • Coordinate with CRAs and RSU on the preparation, handling, and distribution of Clinical Trial Supplies and maintain tracking information.
  • Manage the tracking and management of Case Report Forms (CRFs), queries, and clinical data flow.
  • Serve as a central contact for the clinical team for project communications, correspondence, and documentation.
  • Mentor less experienced Clinical Trial Assistants (CTAs).
  • Assist with training and onboarding of new CTAs.
  • May serve as a subject matter expert for business processes.
  • Potentially lead CTA study teams.
  • Assist with interviewing and screening potential new team members.
  • May accompany CRAs on site visits to assist with clinical monitoring duties after training.
  • Participate in departmental quality or process improvement initiatives.
  • QualificationsHigh School Diploma or equivalent required.
  • At least 5 years of administrative support experience.
  • Equivalent combination of education, training, and experience acceptable.
  • Minimum two years clinical research experience preferred.
  • Proficiency in Microsoft Word, Excel, and PowerPoint.
  • Effective written and verbal communication skills, including good command of English.
  • Strong time management and organizational skills.
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
  • Knowledge of GCP and ICH guidelines as provided in company training.
  • Knowledge of applicable protocol requirements from company training.
  • IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries.
  • We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.
  • Learn more at #J-18808-Ljbffr

Informações Adicionais

  • Quantidade de Vagas 1
  • Jornada Não Informado
 

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