(associate) Clinical Project Manager - Sponsor Dedicated (fixed-term Contract For 6 Months)

IQVIA

Paris, France
Ich-gcp and regulatory compliance
Manage clinical trial execution
Clinical trial budget management
Manage the execution of clinical studies or assigned portion of Phase II - III clinical studies, including orchestration of local trial team

Job Summary

  • Manage the execution of clinical studies or assigned portion of Phase II - III clinical studies, including orchestration of local trial team.
  • Ensure compliance with ICH-GCP and all other relevant regulatory regulations as well as accordance with client SOPs and values.
  • Set up, manage, and review operating unit trial budget to ensure appropriate level of financial oversight and timely budget updates based on trial changes.

Matching Summary

Manage the execution of clinical studies or assigned portion of Phase II - III clinical studies, including orchestration of local trial team.

Skills & Requirements

Must-have

  • ICH-GCP and regulatory compliance
  • Manage clinical trial execution
  • Clinical trial budget management
  • Vendor management
  • Fluent French (C1) and English

Nice-to-have

  • Therapeutic area knowledge
  • Organizational improvement initiatives
  • Influence business partners

Key Requirements

  • Master's or higher-level degree in life science
  • 2 years clinical trial management experience
  • Knowledge of GCP and ICH guidelines
  • Familiar with Veeva CTMS/TMF

Work Rights

Not specified

Tailored Resume

Cover Letter