Regulatory COM
IQVIA(1 month ago)
About this role
Position within IQVIA’s Regulatory & Site Activation unit focused on supporting the regulatory lifecycle of multi-regional clinical studies. The role centers on ensuring compliant study initiation and ongoing regulatory maintenance while enabling business development and study governance. It involves collaboration with cross-functional teams and regional stakeholders to align regulatory strategy and program objectives.
Required Skills
- Negotiation
- Communication
- Project Management
- Regulatory Strategy
- Regulatory Writing
- GCP
- ICH Guidelines
- Clinical Trials
- CTMS
- Quality Management
+3 more
Qualifications
- Bachelor's Degree in Life Sciences
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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