Remote Central Monitoring Analyst – Philippines

Indero (formerly Innovaderm); Philippines; Remote; PHP 502,000 - 781,000; Full time

Benefits offered by this job

Flexible work schedule

Permanent full-time position

Ongoing learning and development

Job summary

Indero in the Philippines is seeking a Central Monitoring professional to perform centralized statistical reviews of study data from start to lock, applying RBQM principles to identify trends and risks. You will collaborate with senior team members to ensure documentation and timely risk management.

This home-based, full-time role requires a Bachelor's in clinical research and at least 1 year of central monitoring or related experience in clinical operations and data management.

Qualifications

• Fluent in English with excellent written and oral communication.
• Experience with central statistical monitoring or RBQM is preferred.
• Understanding of clinical study management and regulatory operations.

Responsibilities

• Follow procedures for review of clinical trial data using various tools in line with the centralized monitoring plan.
• Identify data quality trends indicating systematic errors and potential risks with support from senior team.
• Ensure review results are documented per procedures.
• Support Central Monitoring teams with timely, high-quality reviews.
• Contribute input to risk characterization and reporting.
• Assist in review setup including updating databases and pulling reports.
• Share responsibility for data quality at study, country, and site levels.

Skills

Fluent English

Descriptive analysis basics

Data interpretation

Strong communication

Education

Bachelor’s degree in a field relevant to clinical research

Tools

EDC

IRT

CTMS

MS Office

Job description

Indero in the Philippines is seeking a Central Monitoring professional to perform centralized statistical reviews of study data from start to lock, applying RBQM principles to identify trends and risks. You will collaborate with senior team members to ensure documentation and timely risk management.

This home-based, full-time role requires a Bachelor's in clinical research and at least 1 year of central monitoring or related experience in clinical operations and data management.