About Johnson & Johnson
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

Role Overview
We are searching for the best talent for a Senior Analytical Monitor in our Integrated Data Analytics and Reporting (IDAR) business - experienced individual contributors with strong knowledge of site monitoring and Analytical Risk Based Monitoring (ARBM) practices, data analytics, methods, processes, and technologies. The head office location is in High Wycombe, Buckinghamshire, UK, and this positions is hybrid (3 days onsite weekly), supporting our EMEA team. Note: our office relocates to Maidenhead in October 2026.

Empowered by technology, optimized processes and targeted data analytics, Analytical Monitors will enable Site Managers to dedicate a greater proportion of their time for meaningful engagement with sites, driving improved performance, data reliability and site satisfaction. The Senior Analytical Monitor is accountable for executing processes and activities for multiple clinical trials in conformance to all relevant laws, regulations, guidelines, policies, and procedures.

Key Responsibilities

• Conducting activities in compliance with J&J and functional SOPs, processes and policies.
• Supporting innovation or process improvement projects which may include but are not limited to requirements development, user acceptance testing and identification of improvements to existing and new analytical tools.
• Facilitating smooth and effective communication, managing multiple communication streams and influencing key cross functional stakeholders.
• Performs analytical monitoring activities for clinical trials within assigned scope of responsibility in line with portfolio timelines and priorities.
• Conducts regular reviews at site and subject level that will help early detection of issues and prevent recurrence.
• Collaborates closely with the Site Manager and Central Monitoring Manager to action trends and signals detected at the site and subject level.
• Uses various systems, databases and reporting tools to identify potential risks related to site and subject level data quality, study participant safety, and compliance.
• Provides timely analytical data insights to support the Site Managers in making decisions on site prioritization and critical engagement.

Qualifications & Requirements

• Bachelor's degree or equivalent professional experience is required, preferably in Health Sciences or Data Sciences. Advanced degrees preferred.
• Minimum 8-12 years of experience in Pharmaceutical, CRO or Biotech industry or related field.
• Must be able to work onsite 3 days per week @ High Wycombe / Maidenhead.
• Knowledge of trial site operations and study execution.
• Strong knowledge of regulatory guidelines (e.g., ICH-GCP).
• Demonstrated strong understanding of data analysis and familiarity with basic statistical concepts and hands-on experience using data visualization tools.
• Project, Issue, and risk management experience with strong ability to apply critical thinking & problem-solving skills.
• Strong experience working with technology platforms and systems used for the collection, analysis and reporting of data.

Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will be considered for employment without regard to any other characteristic protected by law.