Regulatory And Start Up Specialist

Ivivamedical

Paris, France
Hybrid
Site activation activities
Gcp/ich and regulatory guidelines
French language fluency required
Perform 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/budgetary guidelines

Job Summary

  • Perform 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/budgetary guidelines.
  • 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.
  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Matching Summary

Perform 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/budgetary guidelines.

Skills & Requirements

Must-have

  • Site Activation activities
  • GCP/ICH and regulatory guidelines
  • French language fluency required
  • Single Point of Contact for sites
  • Quality control of documents

Nice-to-have

  • Negotiating and communication skills
  • Challenging ability
  • Local expertise provision

Key Requirements

  • 3 years' clinical research experience
  • Bachelor’s Degree in life sciences
  • Knowledge of applicable regulatory requirements

Work Rights

Not specified

Tailored Resume

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