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Clinical Trials Operations Manager
2 weeks ago
As a Centralized Monitoring Lead at IQVIA, you will be responsible for providing leadership of the centralized monitoring team to achieve the delivery of the project's overall objectives.
You will have particular focus on leading/advising the centralized team towards solutions to clinical risks identified and facilitating successful implementation of those strategies to address the issues.
Key responsibilities include:
- Facilitating efficient and effective review of Site Visit Reports
- Ensuring consistent standards of implementation for quality
- Ensuring subject safety, data integrity, escalation of issues and timely and responsive feedback
Qualifications and Experience
To be successful in this role, you will need:
- Bachelor's Degree in clinical or life sciences, or related field, or medical degree
- Minimum of 5 years of relevant experience or Medical degree with a minimum 4 years of clinical trial experience
- Advanced knowledge of clinical trial conduct and skill in applying applicable clinical research regulatory requirements
About IQVIA
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
