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Nordic Clinical Research Specialist

3 weeks ago

Copenhagen, Copenhagen, Denmark IQVIA Argentina Full time

About the Role

We are seeking an experienced Regulatory and Site Activation Expert to join our team at IQVIA Argentina. As a key member of our clinical research services, you will be responsible for performing tasks at a country level associated with site activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements, and contractual guidelines.

Main Responsibilities:

  1. Conduct Site Visits: Perform site visits to investigate and address any issues related to site activation.
  2. Prepare Regulatory Reports: Prepare and submit regulatory reports to ensure compliance with applicable regulations.
  3. Develop Project Plans: Collaborate with project management team to develop project plans and timelines.
  4. Manage Budgets: Manage budgets and ensure adherence to financial guidelines.
  5. Collaborate with Stakeholders: Work closely with stakeholders, including investigators, sponsors, and project management teams.

Requirements:

  • At least 1 year of clinical research experience.