Attaché(e) de Recherche Clinique (ARC)

Added
22 minutes ago
Type
Full time
Salary
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product management clinical trial monitoring pharmacovigilance capa ich-gcp
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📋 Description

  • Define, implement and follow the monitoring plan using a risk-based approach.
  • Develop study-related documentation for submitting research protocols to local and national ethics
  • Plan and organize monitoring activities according to study budget, schedule and requirements.
  • Depending on the organization: carry out monitoring activities directly as ARC, including site
  • Review and approve monitoring reports.
  • Identify, document and escalate monitoring findings to study teams.

🎯 Requirements

  • Master's degree in public health, biology or equivalent scientific discipline, complemented by
  • A degree in pharmacy or medicine is a plus.
  • Confirmed experience in monitoring phase 2/3 clinical trials, including autonomous conduct of
  • At least 2 years of prior professional experience in limited-resource countries, in a humanitarian
  • Experience with MSF or other NGOs is a plus.
  • Excellent analytical, synthesis, writing and communication skills.

🎁 Benefits

  • 25 days of paid leave + 22 additional days off.
  • Meal vouchers (12 €/day, 60% covered by Epicentre).
  • Health insurance (mutuelle) covered 100%.
  • 50% reimbursement of public transport pass in Ile de France.
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