Vendor & Third Party Management Clinical Project Manager (m/f/d)
Responsibilities
- Act as the main support for Vendor and Third-Party Management (V&TPM)
- Coordinate V&TPM activities and responsibilities with Evidence Generation study teams
- Serve as a central point of coordination with Evidence Generation teams by supporting the V&TPM SPOC role
- Oversee the end-to-end TPM process, including liaison with Legal, qualification, RFP, contracting, and PO management
- Interface with stakeholders and Company functions, providing inputs and updates as needed
- Manage qualification project timelines and proactively alert stakeholders to deviations or risks
- Coordinate the steps for third-party (vendors and non-vendors) due diligence and/or qualification activities as required
- Ensure oversight, completion, and management of third-party due diligence and qualification activities
- Engage and coordinate with stakeholders and third parties to gather required responses and materials for due diligence
- Provide support and coordination for the EPRM process and contribute to the third-party Quality Risk Assessment activities (QRAs)
Profile
- Degree in a life science or healthcare discipline
- Previous experience in clinical vendor management or similar role with a focus on clinical research advantageous
- Clinical Trial/Medical Affairs experience in a pharmaceutical company or a contract research organization is required
- Project management experience in clinical operations in a pharmaceutical company or a contract research organization
- Good knowledge of the regulatory requirements in Clinical Research and drug development
- Understanding of procurement processes and knowledge of clinical external suppliers landscape (CROs, Central Labs, specialty services, eCOA, and new technologies)
- Experience and ability to manage/supervise third parties and external suppliers advantageous
- Good understanding of clinical data systems/platforms and overall integration of clinical data system and processes
- In-depth knowledge of the international pharmaceutical product development process and GxP requirements
- Fluent written and spoken English knowledge
Benefits
- International Environment
- Very Renowned Pharmaceutical Company
About Hays
With over 15 years of experience in the pharmaceutical and chemical industry as well as in 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 experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.
Staffing process for freelance specialists
- Analysis of qualifications
- Telephone or personal interview
- Contact with customers
- Contract with Hays
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1. Analysis of qualifications
We carry out a detailed analysis of your technical qualifications on the basis of your CV, your application documents and your profile.
Contact at Hays
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