Central Monitor Consultant - Global Vendor

Highly Competitive
  1. Permanent
  2. Clinical Scientist
  3. United Kingdom
London, England
Posting date: 29 Jul 2024
61592

This vacancy has now expired. Please see similar roles below...

Proclinical is on the lookout for a dynamic individual with a strong understanding of clinical operations and development requirements, coupled with a knack for data analytics. This role is perfect for someone who is passionate about delivering excellence and driving customer success. As part of our team, you will be working with a Risk Management and Data Quality Oversight solutions provider, focusing on risk planning and operational monitoring. This is an exciting opportunity to be part of a fast-growing, multi-disciplinary, international company.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Provide consultation to clients on our product and offer operational support as needed.
  • Coach study teams in performing Risk Assessment, identifying critical data and processes, and determining KRIs and QTLs.
  • Guide data analysts in reviewing Central Monitoring Platform outputs and assessing identified risks.
  • Summarize findings and communicate results to clients, helping them understand the impact on their data.
  • Assist Client's Risk Coordinator in the Signal Management process, defining follow-up actions and ensuring robust documentation.
  • Support study teams in adopting an approach to clinical trial monitoring that focuses resources on risks impacting patient safety and data quality.
  • Document lessons learned during each client engagement and share with the organization to facilitate cross-study and cross-organization learning.
  • Participate in the continuous improvement and development of product solutions and operational processes.

Key Skills and Requirements:

  • Bachelor's degree or equivalent experience in a scientific or business-related discipline.
  • Experience in Central Monitoring and Risk Management.
  • Previous experience as a clinical research associate is a plus.


If you are having difficulty in applying or if you have any questions, please contact Auxanne Rameix at a.rameix@proclinical.com



Apply Now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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