
Study Manager
4 days ago
We are seeking an experienced Clinical Project Manager to join our team at IQVIA Argentina. As a key member of our clinical operations team, you will be responsible for delivering clinical studies that meet contractual requirements and drive business growth. Your expertise in clinical trial conduct, regulatory requirements, and project management will enable us to bring new treatments to market faster, benefiting patients worldwide.
Key Responsibilities:
- Participate in bid defense presentations, leading smaller, less complex regional studies.
- Develop integrated study management plans with cross-functional teams.
- Execute clinical studies, ensuring compliance with standard processes and policies.
- Manage risk, set objectives, and assess project team performance.
Requirements
To excel in this role, you should have:
- A strong educational background in Life Sciences or a related field.
- Significant experience in clinical project management, preferably in the pharmaceutical industry.
- Excellent knowledge of clinical trials, including therapeutic areas, protocols, and regulatory requirements.
- Superb communication and interpersonal skills, with a proven ability to collaborate with cross-functional teams.
- Ability to make informed decisions, prioritize tasks, and manage competing demands.
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