Beschreibung
- In this position, you will be responsible for providing the operational expertise to one or more cross-functional investigator-initiated studies (IIS) / non-registrational studies to ensure the effective and efficient delivery of all operational aspects of one or more studies through all phases (Planning, Start-up, Conduct, Close-out), following the appropriate quality standards including applicable regulations and contract with partners
Project Manager (m/f/d)
Reference: -en
Start: asap
Duration: 12 MM++
Main tasks:
- Ensure that study protocols of post-launch studies are reviewed by relevant stakeholders to internal processes
- Ensure that all studies are delivered on time, within scope and budget
- Maintain effective working relationships with key personnel from CDMA, Legal, Procurement and Project Management functions
- Liaise with essential functions and Affiliates as needed to ensure smooth support of IIS studies
- Monitor projects to ensure timely completion, within scope and budget
- Track project performance and analyze the successful completion of short and long term goals
- Track study contracting and complete regular follow up with internal and external stakeholders
- Meet budgetary objectives by requesting invoices and make adjustments to project constraints based on financial analysis
- Create and maintain comprehensive project documentation
- Establish and maintain relationships with third parties/vendors
- Manage close relationships with Clinical Research Organizations and other external stakeholders involved in investigator initiated studies
- Coordinate activities between internal stakeholders to ensure flawless execution of projects
- Assist in the definition of project scope and objectives, involving all relevant stakeholders
- Provide regular updates to the business and Medical colleagues about study status and the resulting publications
- Communication of the generated medical value out of the IISs to the internal stakeholders
Main qualifications
- University Degree in Health Care, Life Sciences or Project Management
- Experience in diagnostics, biotechnology and/or pharmaceutical clinical research with responsibilities for managing all major aspects of strategic planning, organization, implementation, and delivery of clinical programs
- Experience within Project Management / Coordination in health care environment
- Strong interpersonal and stakeholder management skills across all levels of an organization and to lead influentially
- Ability to operate and lead efficiently in a global and heavily matrixed and multi-site organization
- Knowledge of Google Suite, MS Office; Skills in Project Management tools
- Excellent knowledge of applicable standards and regulations for clinical trials and laboratory conduct
- Very good oral and written communication and presentation skills in English (C1)
Main advantages:
- Flexible within regular working hours
- You will work in an international environment
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
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