Clinical Study Associate Manager

Position Overview

Parexel has an exciting opportunity for a Clinical Study Associate Manager. In this role, you will support the Clinical Study Lead by managing various aspects of clinical trial delivery, working with both internal teams and external vendors such as CROs.

Key Responsibilities

• Lead and oversee the planning and management of assigned clinical studies
• Contribute to feasibility assessments, risk mitigation, and global study planning
• Oversee study documentation, including CRFs, monitoring plans, and more
• Manage study systems such as CTMS and TMF
• Coordinate vendor engagements, investigator meetings, and study close-out activities
• Support data quality, budget management, and inspection readiness

Requirements

• Bachelor’s degree with a minimum of 4 years relevant experience
• Technical proficiency in trial management systems and MS applications
• In-depth knowledge of ICH GCP and regulatory guidelines
• Strong interpersonal, leadership, and communication skills
• Attention to detail, proactive and effective time management

Key skills/competency

• Clinical Trials
• Project Management
• Documentation
• Risk Assessment
• Vendor Management
• Regulatory Guidelines
• Data Quality
• Communication
• Budget Management
• Inspection Readiness