Analyst, Analytical Monitor

About the Job

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. Learn more at https://www.jnj.com

Job Function:

Data Analytics & Computational Sciences

Job Sub Function:

Clinical Data Management

Job Category:

Professional

All Job Posting Locations:

High Wycombe, Buckinghamshire, United Kingdom

Job Description:

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine

We are searching for the best talent for multiple Analyst, Analytical Monitors in our Integrated Data Analytics and Reporting (IDAR) business - individual contributors at entry level that support the execution of analytical monitoring activities. The head office location is in High Wycombe, Buckinghamshire, UK, and these positions are hybrid (3 days onsite weekly), supporting our EMEA team.

Empowered by advanced technology, streamlined processes, and targeted data analytics, our Analytical Monitors enable Site Managers to spend more of their time on meaningful site engagement — improving performance, strengthening data integrity, and increasing site satisfaction. The Analyst, Analytical Monitor plays a key role in delivering these outcomes by supporting the execution of analytical monitoring activities across multiple clinical trials in full compliance with applicable laws, regulations, guidelines, policies, and procedures. This role operates with regular guidance from the functional manager and subject-matter experts to meet program objectives.

Are you ready to join our team? Then please read further!

You will be responsible for:

• Conducting activities in compliance with J&J functional SOPs, processes, and policies.
• Facilitating smooth and effective communication, managing multiple communication streams, and following agreed escalation pathways where needed.
• Supporting innovation or process‑improvement projects, including participation in requirements development, user acceptance testing, and identifying improvements to existing and new analytical tools.

Analytical Monitor Role-Specific Responsibilities:

• Performing analytical monitoring activities for clinical trials within assigned scope of responsibility in line with portfolio timelines and priorities, including supporting execution and close‑out as outlined in the end‑to‑end process.
• Conducting regular (fit‑for‑purpose) reviews at site and subject level to enable early detection of issues and prevent recurrence.
• Collaborating closely with the Site Manager and Central Monitoring Manager to action trends and signals detected at the site and subject level.
• Accessing various systems, databases, and reporting tools to identify potential risks related to site‑ and subject‑level data quality, study participant safety, and compliance by identifying trends and early warning signals.
• Providing timely analytical data insights to support Site Managers in making decisions on site prioritization and critical engagement.

Principal Relationships:

• Functional contacts in J&J Innovative Medicine include but are not limited to Site Managers and Local Trial Managers.
• Functional contacts within IDAR include but are not limited to Functional Leadership, Central Monitoring, Data Management, Data Acquisition Experts, Clinical Programmers.
• External contacts include but are not limited to External Suppliers.

Education and Experience Requirements:

• Bachelor's degree (e.g., BS, BA) or equivalent
• Approximately 2+ years of professional experience is required, preferably in Health Sciences or Data Sciences.
• Experience with data analysis preferred
• Experience working with technology platforms and systems used for the collection, analysis and reporting of data.
• Ability to collaborate in an environment of cross-functional stakeholders, plan and coordinate tasks effectively.
• Ability to communicate effectively in English (written and verbal).

Preferred

• Knowledge of clinical drug development within the pharmaceutical industry or related industry
• Familiarity with basic risk management, project management, and/or statistical concepts
• Knowledge of Central Monitoring and Risk-based Quality Management (RBQM)/Risk-based Monitoring (RBM)/Quality by Design (QbD) concepts

Benefits:

We offer a competitive salary and extensive benefits package. The health and well-being of our employees is a priority, we have a flexible working environment as we value work-life balance. We offer career development opportunities for those who want to grow and be part of our organisation.

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. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

#LI-Hybrid

Required Skills:

Collaborative Communications, Cross-Functional Teamwork, Health Sciences, Technology Platforms

Preferred Skills:

Advanced Analytics, Analytical Reasoning, Biostatistics, Business Behavior, Clinical Data Management, Clinical Operations, Cross-Functional Collaboration, Database Applications, Data Privacy Standards, Data Savvy, Execution Focus, Good Clinical Practice (GCP), Process Oriented, Project Support, Report Writing, Standard Operating Procedure (SOP)