Regulatory Affairs Officer 1 (13-Months Contract)
IQVIA(22 days ago)
About this role
Regulatory Affairs professional who prepares and reviews regulatory submission documents to support clinical trial and marketing authorization activities for internal and external clients. Works under general supervision providing regulatory support for assigned projects within a life sciences services organization.
Required Skills
- Regulatory Submissions
- Clinical Trials
- FDA Liaison
- Medical Devices
- Project Management
- Communication
- Microsoft Office
- Process Improvement
- Organization
Qualifications
- Bachelor's Degree in Life Science
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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