Senior CRA – Oncology Trials Lead (Paris)

ICON

Paris

Sur place

EUR 70 000 - 90 000

Plein temps

Il y a 5 jours
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Générateur de candidature

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Avantages offerts par ce poste

Health insurance
Annual leave entitlements
Retirement planning
Life assurance
Employee assistance program

Résumé du poste

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re committed to an inclusive environment and driving innovation in clinical development. ICON seeks a Senior CRA based in Paris to oversee monitoring activities and ensure adherence to protocol and regulatory requirements.

As a Senior CRA, you will lead monitoring tasks on oncology trials, guide others, and travel up to 60% as needed to sites across the Paris region and beyond.

Qualifications

  • Bachelor's degree in a relevant scientific discipline or healthcare field.
  • Extensive experience as a Clinical Research Associate on phase II/III oncology trials.
  • Ability to manage multiple sites and projects with strong organizational skills.
  • Expertise in monitoring practices, data integrity, and site management.

Responsabilités

  • Monitor clinical trial sites for protocol, regulatory, and GCP compliance.
  • Conduct site visits to assess performance and resolve issues.
  • Collaborate with cross-functional teams to ensure timely data collection and reporting.
  • Provide training to site staff to maintain high standards of conduct.
  • Build and maintain relationships with site personnel and stakeholders.

Connaissances

Clinical monitoring
Oncology trials
Data integrity
English & French

Formation

Bachelor's degree in science/healthcare

Outils

Clinical trial software

Description du poste

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re committed to an inclusive environment and driving innovation in clinical development. ICON seeks a Senior CRA based in Paris to oversee monitoring activities and ensure adherence to protocol and regulatory requirements.

As a Senior CRA, you will lead monitoring tasks on oncology trials, guide others, and travel up to 60% as needed to sites across the Paris region and beyond.

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