Site Activation Specialist

2 semanas atrás

São Paulo, São Paulo, Brasil beBeeActivation Tempo inteiro R$42.000 - R$54.000

Job Summary

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Site Activation Specialist - Global Healthcare Leader

">
  • ">
  • We are seeking a highly skilled and organized Site Activation Specialist to join our team in the role of Site Activation Specialist - Global Healthcare Leader. As a member of our site activation team, you will be responsible for ensuring seamless site initiation and activation activities globally.">
">Key Responsibilities:">
  1. ">
  2. Under general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and guidelines.">
  3. Perform site activation activities in assigned studies for investigative sites according to applicable regulations, SOPs and work instructions working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary.">
  4. Review documents for completeness, consistency and accuracy under guidance of senior staff.">
  5. Prepare site regulatory documents reviewing for completeness and accuracy.">
  6. Inform team members of completion of regulatory and contractual documents for individual sites.">
  7. Distribute completed documents to sites and internal project team members.">
  8. Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.">
  9. Review track and follow up the progress the approval and execution of documents, regulatory ethics Informed Consent Form (ICF) and Investigator Pack (IP) release documents.">
">Qualifications:">
  • ">
  • High School Diploma or equivalent">
  • 3 years' experience in an administrative environment or equivalent combination of education training and experience">
  • Good interpersonal communication and organizational skills">
  • Good attention to detail">
  • General awareness clinical trial environment and drug development process">
  • Ability to work on multiple projects">
  • Ability to establish and maintain effective working relationships with co-workers managers and sponsors">
">

 

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