Set-up of proposals (incl. cost calculation and resource planning) for existing customers or projects of existing scope
Responsible to coordinate design and review of contracts, MTAs, ethics approvals and other critical documents
Set-up of projects according to SOPs
Coordinate internal resources and external partners for the flawless execution of projects
Ensure that projects are delivered on-time, within scope and budget as agreed with the customer
Main contact (internal and external) in regards to all project specific questions; incl. preparation and realization of project meetings
Use of software applications to monitor project performance and manage changes in project scope, schedule and costs (Microsoft Office, Laboratory Information Management System (LIMS), Enterprise Resource Planning (ERP) and Customer Relationship Management (CRM) software)
Create and maintain comprehensive project documentation
Data management: Setup of projects in LIMS based database including product specifications, electronic workflows and data transfers in cooperation with IT. Setup of data transfer specifications with customer. Execution of data transfers to customer.
Invoicing (ensure the right items are booked and approval of invoices)
Establish and maintain relationships with existing customers / third parties (e-mail, conference calls and physical meetings)
Support and care of the established clientele (e.g. official journeys, delegations)
Final project assessment (monitoring of the timelines and post calculation of the budget, reasons for divergences and ‘Lessons Learned‘ for future projects)
Report and escalate to management on a regular basis and as needed
Literature research
Education/ Qualification Requirements:
PhD in natural sciences or Master degree in natural sciences with at least two years of experience in clinical study project management
Several years of professional experience (know how) in biomedical research and in mentoring of clinical trials would be a plus