Remote Clinical Study Manager – Oncology (France)

IQVIA LLC; Paris; À distance; EUR 90 000 - 120 000; Plein temps

Résumé du poste

IQVIA LLC in France is seeking a Clinical Study Manager to oversee operational and scientific aspects of assigned trials from setup to delivery, with work-from-home flexibility within France.

You will lead cross-functional teams, ensure compliance with ICH GCP and local regulations, and collaborate closely with clients to meet study objectives and data quality across therapeutic areas.

Qualifications

• Bachelor degree in related life science field.
• Five+ years of clinical research experience including at least 2 years in PM.
• Strong knowledge of ICH GCP and local regulations.
• Proven ability to lead cross-functional teams to deliver trials on time and within budget.
• Experience in Oncology or Onco-hematology preferred.
• Excellent English and French communication skills.

Responsabilités

• Plan and lead day-to-day monitoring activities for complex studies.
• Ensure country-level study commitments and timely data delivery.
• Provide project oversight and leadership for clinical deliverables.
• Lead and manage clinical teams across sites.
• Support activation of trial sites with local and global staff.
• Monitor quality and address issues with the team.
• Review site visit reports and track action items.
• Identify data-related risks and develop mitigation plans.
• Create and maintain project plans and tools for the team.
• Coordinate training and ensure process consistency across systems.

Connaissances

Project leadership

Cross-functional teams

Clinical monitoring

ICH GCP knowledge

English and French

Training coordination

Formation

Bachelor degree in life sciences

Description du poste

IQVIA LLC in France is seeking a Clinical Study Manager to oversee operational and scientific aspects of assigned trials from setup to delivery, with work-from-home flexibility within France.

You will lead cross-functional teams, ensure compliance with ICH GCP and local regulations, and collaborate closely with clients to meet study objectives and data quality across therapeutic areas.