Analyst, Analytical Monitor

Johnson & Johnson; High Wycombe; Hybrid; GBP 60,000 - 80,000; Full time

Job summary

A global healthcare leader is seeking an Analyst/Analytical Monitor to support the execution of analytical monitoring activities for clinical trials. This role focuses on ensuring compliance with regulations while collaborating with cross-functional teams. The ideal candidate has a Bachelor's degree, around 2 years of experience, and a strong background in data analysis. The position is hybrid, requiring 3 days onsite in High Wycombe, offering a competitive salary and benefits for work-life balance.

Benefits

Competitive salary

Flexible working environment

Career development opportunities

Qualifications

• Approximately 2 years of professional experience in Health Sciences or Data Sciences.
• Experience with data analysis preferred.
• Ability to communicate effectively in English, written and verbal.

Responsibilities

• Conduct activities in compliance with J&J functional SOPs, processes, and policies.
• Support innovation or process-improvement projects.
• Provide timely analytical data insights to support decisions on site prioritization.

Skills

Data analysis

Effective communication

Cross-functional collaboration

Education

Bachelor's degree (BS/BA) or equivalent

Tools

Technology platforms for data collection

Job description

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. We aim to make treatments smarter, less invasive, and our expertise in Innovative Medicine and MedTech positions us uniquely to innovate across the full spectrum of healthcare solutions today, delivering breakthroughs of tomorrow to profoundly impact health for more people.

Job Function

Data Analytics & Computational Sciences

Job Sub Function

Clinical Data Management

Job Category

Professional

Location

High Wycombe, Buckinghamshire, United Kingdom (hybrid: 3 days onsite weekly)

Job Description

We are searching for multiple Analyst/Analytical Monitors in our Integrated Data Analytics and Reporting (IDAR) business. These individual contributors will support the execution of analytical monitoring activities for clinical trials, ensuring compliance with applicable laws, regulations, guidelines, policies, and procedures. The role operates under regular guidance from the functional manager and subject‑matter experts to meet program objectives.

Key Responsibilities

• Conduct activities in compliance with J&J functional SOPs, processes, and policies.
• Facilitate smooth and effective communication, managing multiple communication streams and following agreed escalation pathways.
• Support innovation or process‑improvement projects, including participation in requirements development, user acceptance testing, and identifying improvements to existing and new analytical tools.
• Perform analytical monitoring activities for clinical trials within the assigned scope, supporting execution and closeout as outlined in the end‑to‑end process.
• Conduct regular (fit‑for‑purpose) reviews at site and subject level to enable early detection of issues and prevent recurrence.
• Collaborate closely with the Site Manager and Central Monitoring Manager to action trends and signals detected at the site and subject level.
• Access various systems, databases, and reporting tools to identify potential risks related to site/subject data quality, study participant safety, and compliance by identifying trends and early warning signals.
• Provide timely analytical data insights to support Site Managers in making decisions on site prioritization and critical engagement.

Principal Relationships

• Internal: Site Managers, Local Trial Managers, Functional Leadership, Central Monitoring, Data Management, Data Acquisition Experts, Clinical Programmers.
• External: External Suppliers.

Education and Experience Requirements

• Bachelor’s degree (BS/BA) or equivalent.
• Approximately 2 years of professional experience, 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 and plan and coordinate tasks effectively.
• Ability to communicate effectively in English, written and verbal.

Preferred Qualifications

• 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 provide a flexible working environment that values work‑life balance and offer career development opportunities for those who want to grow within our organization.

Equal Opportunity Statement

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 provide reasonable accommodation to individuals with disabilities to participate in the application or interview process.