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Site Activation Specialist

2 meses atrás

São Paulo, São Paulo, Brasil Iqvia Argentina Tempo inteiro

Job Summary

The Sr. Site Activation Specialist will perform tasks at a country level associated with Site Activation (SA) activities for North American sites in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.

Key Responsibilities

  • Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.
  • Perform feasibility, site ID, start up and site activation activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members.
  • Prepare site documents, reviewing for completeness and accuracy.
  • Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
  • Review and provide feedback to management on site performance metrics.
  • Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.
  • Inform team members of completion of feasibility, site ID, regulatory and contractual documents for individual sites.
  • Review, track and follow up the progress, the approval and execution of documents, questionnaires, CDA/SIF, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.
  • Provide local expertise to SAMs and project team during initial and on-going project timeline planning.
  • Perform quality control of documents provided by sites.
  • May have direct contact with sponsors on specific initiatives.

Requirements

  • Bachelor's Degree in Life Science or related field
  • Around 3-4 years clinical research experience, with mandatory experience in the site activation and regulatory department (experience working with the US and Canada is desirable)
  • Advanced level of English (you'll be working with sites in North America)