Regulatory and Clinical Research Associate

Há 2 dias


São Paulo, São Paulo, Brasil beBeeRegulatory Tempo inteiro R$74.180 - R$148.140
Site Activation Specialist

The Site Activation Specialist is responsible for executing feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional or country level. They prepare and manage site documentation; review and negotiate site documents and contracts with sites and sponsors; maintain, review, and report on site performance metrics; serve as the primary point of contact for investigative sites; track completion of appropriate documents for sites; ensure contracts are fully executed; and establish project timelines.

Key Responsibilities
  1. Execute feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements.
  2. Prepare and manage site documentation.
  3. Review and negotiate site documents and contracts with sites and sponsors.
  4. Maintain, review, and report on site performance metrics.
  5. Serve as the primary point of contact for investigative sites.
Requirements
  1. Bachelor's Degree in Life Sciences or a related field.
  2. 1-2 years of experience in clinical research regulatory.
  3. Great communication skills and ability to work in a team.


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