Regulatory and Start Up Manager, IQVIA MedTech, Portugal
IQVIA(3 months ago)
About this role
This role leads the end-to-end management of site activation, maintenance, and regulatory activities for clinical studies or multi-protocol programs. It focuses on coordinating multi-regional trial start-up and ongoing approvals while partnering with internal teams and external stakeholders to enable timely study execution. The position sits within IQVIA’s global clinical research organization supporting life sciences clients.
Required Skills
- Site Activation
- Regulatory Affairs
- Clinical Trials
- Study Start-Up
- Project Management
- Budget Management
- Resource Planning
- CTMS
- Regulatory Strategy
- Submissions
+10 more
Qualifications
- Bachelor's Degree in Life Sciences or Related Field
About IQVIA
iqvia.comIQVIA is a leading global provider of data, technology, and advanced analytics focused on transforming healthcare and life sciences. The company empowers organizations to accelerate innovation, enhance patient outcomes, and expedite the market introduction of new treatments through comprehensive healthcare analytics and real-world evidence. With a commitment to Human Data Science, IQVIA combines its extensive expertise with innovative technology to improve health outcomes worldwide.
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