Central Risk Monitor

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

📋 Description

• Perform remote evaluations and analyses of clinical trial data to detect trends, anomalies, and potential risks impacting patient safety and data integrity.

• Work collaboratively with site staff and clinical teams to address findings from centralized monitoring activities and implement necessary corrective and preventive measures.

• Leverage advanced data analytics tools and technology platforms to improve the efficiency and effectiveness of centralized monitoring processes.

• Offer support and advice to study teams regarding centralized monitoring methodologies, best practices, and regulatory standards.

• Assist in the development and enhancement of centralized monitoring strategies and protocols to ensure optimal data quality and compliance throughout clinical trials.

⛳️ Requirements

• Bachelor’s degree in life sciences, computer science, or a related field.

• Prior experience in clinical research, data management, or monitoring within the pharmaceutical, biotechnology, or CRO sectors.

• Strong grasp of clinical trial processes, regulations, and guidelines (e.g., ICH GCP, FDA regulations).

• Exceptional analytical and critical thinking abilities, with a talent for identifying patterns, trends, and discrepancies in clinical trial data.

• Strong communication and interpersonal abilities, with the capacity to collaborate across functions and convey complex concepts to a variety of stakeholders.

• Openness to travel as needed (approximately 5%).

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career pathways.