Regulatory and Start Up Manager
IQVIA(1 month ago)
About this role
Lead and manage site activation, maintenance and regulatory activities for assigned clinical studies and multi-protocol programs, ensuring timely study initiation and compliance with regulatory requirements. Provide specialist regulatory and scientific support to business development and study teams, and contribute regulatory intelligence and strategy for submissions and approvals. Fluent Arabic is required and finance/budgeting experience is a benefit.
Required Skills
- Regulatory Strategy
- Site Activation
- Clinical Trials
- GCP
- ICH Guidelines
- Technical Writing
- Project Management
- Budget Planning
- CTMS
- Stakeholder Management
+1 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.
View more jobs at IQVIA →Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at IQVIA
Similar Jobs
Clinical Research Associate (Start Up) - Oncology - Los Angeles, CA
Clinical Careers Page(21 days ago)
Regulatory and Start Up Specialist
Precision for Medicine(6 days ago)
Study Start Up Associate II
Clinical Careers Page(12 days ago)
Site Activation Partner III - FSP
Parexel(1 month ago)
Senior Study Start-up Specialist
BeOne Medicines(19 days ago)
Start Up Manager
Clinical Careers Page(3 months ago)