Analyst II, Analytical Monitor

Hobson Prior International Ltd; Greater London; Hybrid; GBP 40,000 - 55,000; Full time

Job summary

A leading life sciences recruitment firm is seeking an experienced Analyst to join their dynamic team in London. This hybrid position involves using data analytics to enhance clinical trial monitoring processes, ensuring data quality and compliance. Candidates should have a Bachelor's Degree in health or data sciences, alongside strong problem-solving and collaboration skills. The role offers a chance to contribute to innovative solutions in clinical trials.

Qualifications

• Familiarity with clinical trial operations and regulatory guidelines (e.g., ICH-GCP).
• Experience with data analysis concepts.
• Knowledge of risk-based monitoring and quality management techniques is a plus.

Responsibilities

• Review and analyze clinical trial data to identify potential risks and trends.
• Collaborate with Site Managers to address issues and improve site performance.
• Ensure all activities comply with relevant guidelines, policies, and regulations.

Skills

Data analysis

Problem-solving

Critical thinking

Project management

Collaboration

Education

Bachelor's Degree in health sciences, data sciences, or related field

Tools

Technology platforms for data collection

Job description

Overview

Experienced in Analytics and looking for your next move into a monitoring position? This UK based position is perfect for you!

Hobson Prior is seeking dedicated Analyst to join a dynamic team supporting clinical trials across the EMEA region. In this role, you will use data analytics to enhance site monitoring processes, ensuring data quality, participant safety, and compliance. This hybrid position requires collaboration with cross-functional teams and offers an opportunity to contribute to innovative approaches in clinical trial monitoring.

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

Responsibilities

• Review and analyze clinical trial data to identify potential risks and trends.
• Collaborate with Site Managers to address issues and improve site performance.
• Use various systems and tools to monitor data quality and compliance.
• Provide insights to support decision-making and prioritize site engagement.
• Support process improvement projects, including testing and tool enhancements.
• Ensure all activities comply with relevant guidelines, policies, and regulations.

Key Skills and Requirements

• Bachelors Degree alongside a background in health sciences, data sciences, or a related field.
• Familiarity with clinical trial operations, regulatory guidelines (e.g., ICH-GCP), and data analysis concepts.
• Experience with technology platforms for data collection, analysis, and reporting.
• Strong problem-solving, critical thinking, and project management skills.
• Ability to collaborate effectively with cross-functional teams and communicate clearly in English.
• Knowledge of risk-based monitoring, quality management, and data visualization techniques is a plus.

For more information, please contact Bobby Burke.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

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

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