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About the role
- Senior Global Trial Manager leading clinical trial delivery at IQVIA. Overseeing multi-regional studies and managing clinical teams to meet project objectives and regulatory compliance.
Responsibilities
- Ensure clinical delivery of assigned projects in compliance with regulatory requirements
- Accountable for meeting projects’ Clinical targets
- Contribute to the development of the project risk mitigation plan
- Manage clinical risks through the project lifecycle
- Ensure clinical quality delivery by identifying quality standards/requirements
- Monitor and manage changes against Study work plan (SWP)
- Work as the primary Point of contact for the customer project manager
- Identify clinical stakeholder landscape for the project
- Collaborate with the clinical team to support milestone achievements
- Report to internal and external stakeholders as per project scope requirements
- Manage the clinical team at project level to successfully deliver the project
Requirements
- Typically requires 3 - 5 years of prior relevant experience
- Bachelor’s degree in health care or other scientific discipline required
- Requires 7 years clinical research/monitoring experience or equivalent combination of education, training and experience
- Requires consolidated knowledge and understanding of Project management practices and terminology
- Requires good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Requires broad protocol knowledge and therapeutic knowledge
- Requires good understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates
- Requires understanding of project finances to oversee the clinical/monitoring budget and changes to scope.
Benefits
- Incentive plans
- Bonuses
- Health and welfare benefits
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