Clinical Monitoring Analyst

This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• Assist the Centralized Monitoring Lead in crafting tailored centralized monitoring strategies.

• Play a role in recognizing centralized monitoring components, such as QTLs, KRIs, data visualizations, and Data Quality Assessments.

• Configure and program QTLs, KRIs, and Data Quality Assessments in alignment with the study CMP.

• Update the Centralized Monitoring Platform at specified intervals to facilitate signal detection.

• Create and maintain specifications for the Centralized Monitoring Platform and ensure their filing in the eTMF.

• Review and comprehend study protocols.

• Grasp the study data sources, data transfer specifications, and data structures.

• Conduct and document peer reviews of platform setups performed by other CMA colleagues.

• Collaborate directly with the client on a sponsor-specific project and oversee deliverables.

⛳️ Requirements

• Minimum of 3 years of relevant experience in pharmaceutical research and development or a related field, ideally in centralized monitoring, data management, and/or biostatistics.

• 2–3 years of experience with SAS, including proficiency in macro language.

• Familiarity with Cluepoints.

• Capability to work independently and interact effectively with relevant stakeholders.

• Understanding of basic statistical analysis concepts and the ability to interpret results.

• Commitment to maintaining the confidentiality of data and information.

• Ability to operate with minimal close supervision.

• Proven communication, interpersonal, organizational, and problem-solving skills.

• High levels of initiative, motivation, and dedication.

• Previous experience in a Data Management-related role.

• Knowledge of relational databases, ideally Clinical Data Management and EDC Systems.

• Experience in communicating with personnel at all levels and participating in collaborative teams, both locally and globally.

• Advanced understanding of federal regulations, Good Clinical Practice, and Good Clinical Data Management Practices.

• Exceptional verbal and written proficiency in English.

• Not eligible for UK visa sponsorship.

🏝️ Benefits

• Comprehensive health and wellness programs.

• Opportunities for professional development and training.

• Competitive salary and performance-based incentives.

• Flexible working hours and remote work options.