Senior Clinical Project Manager
- To perform, manage, and coordinate the setup and running of clinical trials in accordance with the protocol, Richmond SOPs, GCP, and all relevant guidelines.
- Acting as the main point of contact for sponsors, vendors, and the wider project team.
- Ability to help with trial design by liaising directly with sponsors and PI, integrate information from a range of sources and critically evaluate it, identify the implications and making appropriate decisions (e.g. about study design and timing).
- Quality check and coordinate flow of all study documents, ahead of study initiation.
- Check meeting agendas, minutes, documents, and scheduling.
- Coordinate external and internal study meetings, as required.
- Supervise/mentor CRS and CPMs within teams, as required.
- Maintain and quality control the Investigator Site File.
- Ensure effective close out activities.
- Manage resolution of data queries to facilitate timely database lock and reviews of study reports, ahead of submission to regulatory authority.
- Undertake continuous improvement activities in relation to further improving processes and work culture.
- BSc in Life Sciences (or equivalent); or other clinical research academic qualification (e.g., MSc, Post Grad Diploma etc.)
- Previous experience working in a Clinical Project Management position
- Ability to communicate professionally and appropriately with external clients and internal professionals.
- Excellent communication skills, both written and verbal.
- Strong fundamental knowledge in project management methodologies, principles and demonstrable practical exposure.
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