Implementation Consultant

Pop Science Ltd; Cambridge; Remote; GBP 50,000 - 70,000; Full time

Job summary

A leading company in the clinical trials industry is seeking a Risk Based Quality Management Implementation Consultant. This remote role involves collaborating with study teams, defining Key Risk Indicators, and enhancing clinical trial quality through data management. Ideal candidates will have SQL programming skills and a passion for innovative system development.

Qualifications

• Experience in clinical data management or as a SQL programmer.
• Excited about implementing centralized monitoring processes.

Responsibilities

• Collaborate with client teams to define Key Risk Indicators.
• Create technical design specifications for data extraction.
• Deliver projects within established timelines.

Skills

SQL

Data Management

Risk Management

Job description

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Job Opportunity: Risk Based Quality Management Implementation Consultant (Data Manager)

Are you a SQL programmer or clinical data manager who loves building innovative systems and is looking to transition into technology? We have a great remote opportunity, though our client's offices are in Cambridge.

Our client is rapidly growing due to the success of their industry-leading products. We are seeking an Implementation Consultant who wants to apply their knowledge and experience to create a cutting-edge web application for the clinical trials industry.

Ideally, you will be excited about leading the implementation and development of centralized monitoring processes, engaging directly with senior leadership, and contributing to an application that advances medical treatments for patients.

Responsibilities:

1. Collaborate with client study teams to define and design Key Risk Indicators (KRIs) and data visualizations.
2. Work with client data teams to gather requirements.
3. Create requirement and technical design specifications for data extraction and aggregation routines.
4. Coordinate with development during the build cycle to ensure SQL stored procedures meet the data needs for dashboards, including setting up and executing SQL queries.
5. Review the study build with the client and accept the build prior to validation.
6. Deliver projects within established timelines.
7. Potentially perform periodic centralized monitoring reviews to analyze study and site risk profiles and recommend actions based on insights and experience.

This role offers a great chance for someone interested in leveraging data to enhance clinical trial quality by identifying predictive leading indicators of risk. While there is a technical aspect to the build cycle, there is also an opportunity to gain practical experience in RBQM and develop critical thinking skills.