FSP Sponsor Dedicated - Study Start-Up Manager
IQVIA(1 day ago)
About this role
This role involves overseeing the delivery of site activation, maintenance, and regulatory activities for clinical trials within a pharmaceutical or life sciences company. The responsibilities include managing project timelines, regulatory strategies, compliance, and collaboration across teams, with an emphasis on technical and regulatory support for successful study initiation and maintenance.
Required Skills
- Regulatory Strategy
- Clinical Trials
- Project Management
- GCP
- ICH Guidelines
- Regulatory Compliance
- Biotechnology
- Healthcare Industry
- Contract Negotiation
- Team Leadership
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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