# Clinical Trial Manager II

**Company**: IQVIA Biotech
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Kirkland-Quebec-Canada/Gestionnaire-d-essais-cliniques-II-CTM-II--IQVIA-Biotech_R1571601?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_81668a3d-c25

## 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
- Good Clinical Practice (GCP)
- International Conference on Harmonisation (ICH) guidelines
- project management
- clinical research
- monitoring

### Nice to have
- oncology experience
- global perspective

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Kirkland-Quebec-Canada/Gestionnaire-d-essais-cliniques-II-CTM-II--IQVIA-Biotech_R1571601?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)