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From the employer's careers site First seen 26 Oct 2026

Clinical Trial Manager II

IQVIA Biotech senior full-time

The employer hasn't listed a salary.

Apply on IQVIA Biotech

Description

IQVIA Biotech is seeking a Clinical Trial Manager with oncology experience and a global perspective.

As a Clinical Trial Manager, you will play a vital role in the conduct of clinical trials. You will work closely with clinical teams to contribute to improving patients' lives by accelerating the commercialization of new medicines.

Key Responsibilities:

  • Ensure the execution of clinical trials for assigned projects, in accordance with regulatory requirements, client requirements, and internal requirements.
  • Identify and manage project clinical stakeholders, both internal and external, through effective communication and rigorous issue management.
  • Collaborate with the clinical team to achieve established objectives and report to internal and external stakeholders as required by the project.
  • Plan the clinical team's resources and talent, and coach the clinical team at the project level to ensure its success.
  • Lead regular team meetings and communicate effectively to achieve objectives.
  • Contribute to professional development by providing feedback to the clinical team's frontline managers on their performance against project tasks.
  • Participate in the development of the clinical delivery strategy for proposals and develop and present the clinical operations plan.
  • May mentor and train new colleagues during their onboarding.
  • May act as a lead clinical manager alongside other clinical managers for the execution of large-scale international clinical trials.
  • May participate in site visits, as required, to support project execution.

Requirements:

  • Bachelor's degree in health sciences or another scientific discipline required.
  • 5 years of experience in clinical research/monitoring or an equivalent combination of education and experience required.
  • Basic knowledge of project management practices and terminology required.
  • Sound knowledge of regulatory requirements applicable to clinical research, including Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines.
  • In-depth knowledge of protocols and therapeutic aspects.
  • Understanding of the financial aspects of projects.

What We Offer:

  • Competitive salary
  • Opportunity to work with a leading global provider of clinical research services, commercial insights, and healthcare intelligence
  • Collaborative and dynamic work environment

IQVIA is an equal opportunity employer and welcomes applications from all qualified candidates.

Skills

Required

Nice to have

  • oncology experience
  • global perspective
Apply on IQVIA Biotech