Clinical Trial Manager - Single Sponsor Dedicated

IQVIA

France
Ich-gcp and regulatory compliance
Clinical trial protocol execution
Trial recruitment and timelines
Manage wide span of phases of clinical research projects in various therapeutic areas and cooperate closely with one of our key clients

Job Summary

  • Manage wide span of phases of clinical research projects in various therapeutic areas and cooperate closely with one of our key clients.
  • Accountable for the operational management of the component of clinical trials, assuring achievement of trial recruitment commitment, timelines, budget and quality standards.
  • Ensures all tasks are carried out in accordance with respective applicable SOPs, Business Practices, and regulatory requirements, maintaining the highest ethical and professional standards.

Matching Summary

Manage wide span of phases of clinical research projects in various therapeutic areas and cooperate closely with one of our key clients.

Skills & Requirements

Must-have

  • ICH-GCP and regulatory compliance
  • clinical trial protocol execution
  • trial recruitment and timelines
  • vendor management
  • site relationship management

Nice-to-have

  • strategic thinking
  • solution orientation
  • growth mindset
  • driving transformation

Key Requirements

  • Master's or higher-level degree
  • at least 2 years clinical trial management experience
  • at least 2 years monitoring experience in France
  • fluent English and French language skills

Work Rights

Not specified

Tailored Resume

Cover Letter