Beschreibung
Clinical Vendor Manager (w/m/d) in Basel, SwitzerlandLocation: Basel, Switzerland
Duration: 1 year
We are seeking a highly qualified individual to join our team as a Third-Party Qualifications Specialist, focusing on Research & Development. This is a new hire role aimed at expanding our capabilities in managing third-party relationships. The successful candidate will be responsible for driving due diligence and qualification activities for both vendor and non-vendor third parties. This role plays a critical part in ensuring compliance with regulatory requirements and maintaining the quality of our third-party relationships.
Tasks:
- Drive third-party due diligence and qualification activities, ensuring oversight, completion, and management according to the nature and type of third-party activities.
- Accountable for the quality and completeness of due diligence/qualifications and associated documentation in Third-Party Management (TPM) systems and tools.
- Engage and coordinate with third parties to obtain necessary materials/information for due diligence activities.
- Identify potential risks associated with third parties and contribute to the risk management process.
- Support the third-party governance and oversight process, including Quality Risk Assessments (QRAs) for various GMA activities.
- Lead the deviation management process for External Relations Management Medical Affairs, including investigation, documentation, and CAPA implementation.
- Coordinate the maintenance of the due diligence tool (TPIAT).
- Contribute to the continuous improvement of the global GMA TPM process, including the design, revision, and implementation of standards and policies.
- Provide expertise and training on TPM to operational teams and countries.
- Collaborate with various stakeholders, including ESP Quality Assurance, Procurement, and VPG, as needed.
- Ensure compliance with all required SOPs and business guidance documents.
Requirements:
- Degree in a life science or healthcare discipline.
- Previous experience in clinical vendor management or a similar role with a focus on clinical research.
- Experience in clinical trial/medical affairs in a pharmaceutical company or contract research organization.
- Experience in strategic negotiations, alliances, and operations in the pharmaceutical industry.
- Good knowledge of regulatory requirements in clinical research and drug development, including GxP requirements, quality management systems, and relevant Health Authority regulations.
- Understanding of procurement processes and knowledge of the clinical external suppliers landscape.
- Experience in managing/supervising third parties and external suppliers.
- Understanding of clinical data systems/platforms and their integration.
- Fluent written and spoken English proficiency.
If this role is of interest to you, or anyone from your network, feel free to send me your CV or alternatively, give me a call under and expected hourly rate for immediate consideration. I am specialised recruiter taking care of various projects within the Life Sciences Industry.
Sthree Switzerland is acting as an Employment Business in relation to this vacancy.