Site Management Associate

Responsibilities

• Maintain databases and tracking systems to ensure data integrity
• Serve as the primary contact point for sites regarding vendors, study supplies, and access management
• Manage large volumes of documentation, including compiling, processing, and filing
• Coordinate site-specific query resolution and project training
• Facilitate communication between company departments and external investigative sites
• Ensure proper administration of site and vendor payments
• Assist with meeting arrangements, including preparing draft agendas and minutes

Requirements

• College or University Degree in Life Sciences
• Prior administrative experience in a Clinical Research or CRO environment
• Strong organizational, planning, and problem-solving abilities
• Detail-oriented with the ability to multi-task in a fast-paced environment
• Excellent interpersonal and customer service skills

Preferred Qualifications

• Experience working in an international clinical research setting

About the Company

PSI is a leading, privately owned Contract Research Organization (CRO) with over 30 years of experience in the pharmaceutical industry. We are a full-service global partner dedicated to delivering high-quality clinical trials across a broad spectrum of therapeutic indications. At PSI, we pride ourselves on our stability, inclusive culture, and commitment to investing in our people's long-term career growth.