Clinical Trial Manager - Single Sponsor Dedicated

IQVIA

France
Operational management of clinical trials
Ich-gcp and regulatory compliance
Trial recruitment, timelines, budget, quality
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.
  • Lead and support local trial team and investigative sites in timely preparation of required trial documents, contracts, and necessary approvals.

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

  • operational management of clinical trials
  • ICH-GCP and regulatory compliance
  • trial recruitment, timelines, budget, quality
  • site relationship management
  • vendor management

Nice-to-have

  • strategic thinking and solution orientation
  • growth mindset and drive change
  • influencing business partners
  • ethical and professional standards

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