Clinical Trial Project Manager USA
Clinvet
- USA
- $81,000-172,000 per year
- Permanent
- Full-time
- Coordinate FCT across all their phases (e.g., feasibility assessment, quotation, set up, live phase, close-out, reporting, and study master file compilation), liaise with the responsible team members for the services performed within the group, and manage the relationship with external partners and vendors.
- Ensure projects complete their life cycle and deliverables meet the agreed timelines, quality, and cost.
- Report to management and Sponsors on the status of projects, including budgets and timelines, through the implementation and coordination of regular project review meetings.
- Proactively identify risks that might jeopardize projects, e.g., technical feasibility, availability of resources, timely execution, budget constraints, etc.
- Develop and maintain project management tools, including but not limited to Gantt charts, project budgets, forecasts, etc.
- Liaise and coordinate with different departments, partner companies, and external partners to ensure that necessary resources are available to perform the required function at the planned time to achieve the project outcomes.
- Serve as primary project contact with Sponsors to ensure that communication and reporting schedules are followed.
- Develop site training materials including study specific materials and GCP materials.
- Mentor and train fellow team members on FCT management.
- Promote the organization's capabilities and values internally and externally.
- Fulfil Monitor responsibilities within GCP and non-GCP studies, where applicable.
- Contributing to study-level risk assessments.
- Identifying and resolving issues at a global level.
- Leading global study-level documentation and required tool and systems set-up.
- DVM or related Life Sciences degree, accompanied by a minimum of five years of experience in Field Clinical Trials (FCT) and Project Management.
- Ideal candidates should demonstrate industry awareness, including expertise in the pharmaceutical sector, familiarity with FDA/CVM, USDA/CVB, EMA, VICH Guidelines, Clinical Field Trials, and data quality requirements.