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Clinical Operations Consultant (risk based study management)

2020-07-28 16:34:552020-08-24 Pop Science
Job Type Permanent Full Time
Location Cambridge
Area EMEA (other) Cambridge
Sector Clinical Research
Salary £40k - 65k per year
Start Date ASAP
Job Ref 912
Job Views 112
Description

Are you a Clinical Project Manager, CRA, or expert data manager with a passion for using data to help manage risk in your studies? We've got a great Risk Based Quality Management Operations Consultant role, , to work with clients of all sizes and help them progress their risk management strategies. You will also be able to use your knowledge to develop software to support this.

Our client is growing at pace due to the success of their Industry leading products. We are looking for an Industry leading Operations Consultant who wants to apply knowledge and experience to the creation of a leading edge web application for the clinical trials industry.

They are leading global providers of Risk-Based Monitoring (RBM) solutions for clinical trials, and in order to expand its international presence and to keep up with the demand, they need to grow their team.

Role Overview

The RBQM Operations Consultant is a critical role, responsible for working with our customers to operationalise RBQM for clinical studies, including the implementation of our product into their operational practice. This role is a client-facing role and will work alongside the in house team to successfully implement our product into the client effectively, efficiently and to a high-quality standard.

The Role

You will be responsible for:

  • SoW ownership
  • Main liaison with client
  • Delivering to timescales
  • Responsible for project plan, budget and renegotiating statements of works
  • Creation and maintenance of project documentation as applicable to the role
  • Set up and lead kick off meeting
  • Support the performance of the protocol risk assessment, including facilitated risk assessments where contracted
  • Work with the client and in house teams to define risk controls including key risk indicators
  • Work with the client to further define key risk indicators e.g. what does it measure, what questions are you answering, what's the critical thinking around the route cause analysis
  • Support the client with the development of the overall monitoring strategy, including the centralized monitoring plan
  • Performing periodic centralized monitoring review of the Study and Site dashboards to provide insights in study and site risk profile and recommendations for action
  • Complete SOP Gap Analysis work where consulting has been sought from clients
  • Support the internal sales team as required for client RFPs and bid defense meetings
  • Act as internal stakeholder representing clients/end users as part of the software product development cycle.
  • Ongoing service support through the study

This is a great opportunity for someone who is interested in how we can make better use of data in clinical trials to determine which sites, patients and data are most at risk with a view to being able to identify the leading indicators that are predictive of study and site quality, and how to operationalize this in every day clinical trial conduct.

Technical Skills (not exclusive)

  • Understanding of risk-based, centralized monitoring, ideally have worked with this methodology but not essential
  • Ability to review clinical protocols and understand the study design and subject visits schedules
  • Ability to apply an appropriate monitoring strategy to a study, based on the outcome of the risk assessment
  • Ability to demonstrate and apply critical thinking to KRI and data visualization design and centralized monitoring implementation
  • Desire to further develop centralized monitoring process and skills
  • Proven experience in managing client relationships/studies

#RBM #centralmonitoring #riskbasedmanagement #riskbasedmonitoring #sql #edc #rave #inform #medidata

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