Clinical Research Monitor - Remote

Overview

The Clinical Research Monitor supports clinical research studies by ensuring compliance with protocols and regulations, managing documentation, and reviewing research data.

In Short

• Monitor protocol and regulatory compliance of clinical research studies.
• Review research data for accuracy and completeness.
• Manage documentation and track study milestones.
• Write detailed monitoring reports for studies.
• Develop risk monitoring plans.
• Communicate with study teams regarding trial activities.
• Assist with data management tasks.
• Ensure compliance with SOPs and GCP guidelines.
• Adapt to changing priorities effectively.
• Maintain regular attendance and meet departmental goals.

Requirements

• Bachelor's degree in a relevant area.
• 2+ years of clinical research experience.
• Prior clinical research monitoring experience preferred.
• Strong understanding of clinical study operations.
• Ability to communicate effectively with diverse audiences.
• Capability to handle data queries and ensure data quality.
• Knowledge of regulatory requirements and ethical considerations.
• Ability to work independently with minimal supervision.
• Strong analytical and problem-solving skills.
• Ability to adapt quickly to changes.

Benefits

• Competitive salary range of $70,720 - $126,880 per year.
• Comprehensive benefits package.
• Opportunity to work remotely.
• Supportive work environment.
• Professional development opportunities.
• Equal Opportunity Employer.
• Commitment to diversity and inclusion.
• Flexible work arrangements.
• Access to cutting-edge research and resources.
• Collaborative team culture.