Job Description

ProPharma Group seeks a Senior Central Monitor to support remote clinical monitoring activities for pharmaceutical and biotech studies. The role involves centralized data management, site oversight, and coordination with clinical teams to ensure regulatory compliance and study delivery.

Responsibilities

• Perform remote site monitoring and management activities per FDA, ICH GCP, and company SOPs
• Support study monitoring teams in implementing strategies and ensuring quality processes
• Collect data and generate reports on recruitment, enrollment, drug supply, and site payments
• Conduct data risk assessments and support document collection and visit preparation
• Communicate with clinical sites and maintain study team coordination throughout trial duration

Requirements

• Bachelor's degree preferred; comparable training and experience considered
• Minimum 3 years in study coordination, in-house monitoring, or biotech/pharma experience
• Proficiency with clinical trial systems (EDMS, EDC, CTMS)
• Strong communication and interpersonal skills with cross-functional stakeholders
• Excellent organizational abilities and attention to detail
• Knowledge of quality assurance concepts and regulatory guidelines (FDA, ICH GCP)

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