Job Details
Contract Duration – 12 months.
Location – Cambridge or Uxbridge
Remote working – 1 day/month in the office
Rate - £40/hr (Inside IR35)
This project is based on the implementation of a new regulation for IVDR which iis used by the organisation on its products and making submissions for those devices that are under a different regulation.
You are expected to devise how to implement this in the best way and seeing through to the execution phase.
Top Skills:
- Highly Organised
- Detail Orientated
- Strong Communicator
- Smartsheet / SharePoint Experience
- Would be beneficial if they’ve project managed in regulatory or clinical trials.
- Good to have someone from a Pharma / Medical Devices / Healthcare background.
Job Details:
- Manages one or more high-level, complex projects within the constraints of scope, quality, time, and cost, to deliver specified requirements. Projects may be strategic in nature.
- Responsibilities may include resource allocation and all phases of development life cycle (i.e., feasibility study, requirements, analysis, ROI, business plan, design, testing, and implementation planning).
- Regularly interacts with management.
- Coordinates and directs the activities of project team members.
- May be a cross-functional team.
- Ensures all project requirements and/or objectives are documented.
- May obtain and manage external resources required for project completion.
Skills:
- Expertise in running medium to large scale projects, excellent understanding of project management processes and procedures,
- Experience with project management and analyst methodologies and best practices, strong analytical skills, business process development best practices, change management, strong MS Word, MS PowerPoint, MS Excel and remote collaboration / meeting tools (e.g. WebEx) skills, understanding of systems for sharing and collaboration, excellent communication skills to work with cross-program resources