Clinical Associate Regulatory Submissions - IQVIA Biotech
IQVIA(1 month ago)
About this role
IQVIA Biotech is hiring a homebased Clinical Associate focused on regulatory submissions and start-up support for BENELUX countries. The role serves as a key local regulatory point of contact for studies, ensuring country-specific requirements are met and submissions are completed accurately and on time. It operates within a regulated clinical trial environment supporting biotech and emerging biopharma partners.
Required Skills
- Regulatory Submissions
- Site Activation
- CTIS
- EUCTR
- Feasibility
- Start-Up
- Document Review
- Quality Control
- Site Contracts
- Contract Negotiation
+7 more
Qualifications
- BSc in Health 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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