Clinical Monitoring Analyst (Cluepoints) - Remote

Location: Remote from London, United Kingdom

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Support the Centralized Monitoring Lead in developing study-specific centralized monitoring strategies.
• Set up and program quality tolerance limits, key risk indicators, data visualizations, and data quality assessments in Cluepoints.
• Refresh the centralized monitoring platform at predefined frequencies to support signal identification.
• Generate and maintain platform specifications and file documentation in the electronic Trial Master File.
• Review clinical protocols, data sources, transfer specifications, and data structures.
• Perform and document peer reviews of centralized monitoring platform setups.

Requirements

• At least 3 years of relevant experience in pharmaceutical research and development or a related field, preferably in centralized monitoring, data management, or biostatistics.
• 2–3 years of SAS experience, including macro language, and experience with Cluepoints.
• Prior experience in a data management-related field, with relational databases and preferably clinical data management or EDC systems.
• Knowledge of basic statistical analysis concepts and the ability to interpret results.
• Advanced knowledge of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices.
• Excellent verbal and written English; the role is not eligible for UK visa sponsorship.

Culture & Benefits

• Work autonomously with limited close supervision.
• Collaborate directly with the sponsor and stakeholders across local and global teams.
• Maintain confidentiality when handling clinical research data and information.
• Contribute to the development and delivery of clinical study centralized monitoring processes.