Site Activation Coordinator

hace 15 horas


Xico, México Iqvia Argentina A tiempo completo

Job Overview: As a Site Contracts Specialist, you will be responsible for executing the feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional or country level.

Key Responsibilities:

  • Serve as a Single Point of Contact (SPOC) to perform feasibility, site activation, and some maintenance 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.
  • Prepare site documents, reviewing for completeness and accuracy.
  • Inform team members of completion of regulatory, contractual, and other documents for individual sites.
  • Distribute completed documents to sites and internal project team members.
  • Update and maintain internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project-specific information.
  • Review, track, and follow up on the progress, approval, and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents.

Requirements:

  • Bachelor's Degree in Life Sciences or a related field.
  • 1 - 3 years of experience in management, negotiation, drafting, and modification of contracts; budget management.
  • 3 years of experience in a healthcare environment: CROs or Pharma companies.

Salary Range: $60,000 - $80,000 per year



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