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.
- Ensure that project recruitment targets are met and implement appropriate recruitment strategies.
- Contribute to the development of the project risk management plan and manage clinical risks throughout its lifecycle.
- Ensure the quality of clinical trials by identifying quality standards and requirements, planning compliance assessment methods, and monitoring and managing clinical quality issues.
- Manage the clinical aspects of project funding, including the Estimate at Completion (EAC).
- Identify and manage the project's clinical stakeholders, both internal and external, through effective communication and rigorous issue management.
- Collaborate with the clinical team to achieve established objectives.
- Plan the clinical team's resources and talent.
- 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.
- 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
Equal Opportunities Employer:
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, marital status, or any other status protected by applicable law.