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As a Regulatory and Site Activation Manager at IQVIA, you will be responsible for directing and managing the delivery of site activation, maintenance, and regulatory activities for selected studies or multi-protocol programs. Your expertise will be crucial in overseeing the execution of site activation and maintenance, ensuring compliance with project timelines and regulatory requirements.
Key Responsibilities- Develop and implement management plans according to the scope of work and project plan, resolving project-related issues as needed.
- Collaborate with Regulatory & Site Activation teams to deliver project scope in compliance with the IQVIA Management Plan.
- Provide specialist regulatory and technical scientific support to facilitate business development, initiation, and maintenance of clinical trials.
- Assess and review the regulatory landscape, contributing to the collection, interpretation, analysis, and dissemination of accurate regulatory intelligence.
- Execute operational strategy for maintenance of clinical study approvals, authorizations, and review/negotiation of contracts and essential documents.
- Bachelor's Degree in a related field.
- 6 years of clinical research experience, including 3 years in a leadership capacity.
IQVIA is a leading healthcare technology and consulting company that provides innovative solutions to the life sciences industry. As a Regulatory and Site Activation Manager, you will be part of a dynamic team that is dedicated to delivering high-quality services to our clients.
