Are you looking for a pathway to Clinical Project Management? Why not join Covance as a Project Coordinator?
The role includes:
- Working independently
- Owning and developing study specific documents (e.g., Project Management Plan, Communication Plan, Investigator Package Plan, Risk Register, Project Specific Training Matrix and any other applicable plans as required)
- Maintaining an internalstandardised filing structure for study related documents
- Responsibility for project setup activities
- Organising and attend applicable study-related meetings
- Generating presentations
- Developing new ideas
+ University/college degree, preferably in a healthcare/scientific field. Specific clinical research experience may be substituted for education.
+ Knowledge of the clinical trial process with early clinical pharmacology experience preferred.
+ Minimum 2-3 years of experience in a research environment.
+ Minimum 1-2 years of experience working in a project management environment.
+ Knowledge of protocol designs, study objectives, study procedures, and project-related timelines.
+ Knowledge of GCP/ICH Guidelines and applicable Regulatory Authority Guidelines.
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