Clinical Project Manager - Early Phase Trials

Parexel is dedicated to improving the world's health through clinical trials and regulatory consulting. The Clinical Project Manager for Early Phase leads teams to ensure the successful execution of clinical operations and manages project budgets while maintaining compliance with regulations.

Responsibilities:

• Own the sponsor relationship and manage sponsor communication
• Serve as the central point of contact and escalation for functional teams
• Proactively communicate project progress, risks, and solutions to sponsors and internal teams
• Lead regular meetings with sponsors and project teams to ensure objectives are met
• Review relevant materials and attend strategy meetings
• Prepare for Bid Defense and develop project management strategies
• Attend Bid Defense and handover meetings
• Manage study start-up activities and ensure best practices are implemented
• Oversee site selection strategy and review project contracts and budgets
• Set up project teams and systems, and manage IRB/EC and RA approval processes
• Lead internal and sponsor kick-off meetings and ensure team understanding of project scope and expectations
• Lead projects to completion within budget and schedule, ensuring contract specifications are met
• Provide performance feedback and ensure project tracking using CTMS
• Monitor study timelines, recruitment, retention, and data cleaning
• Prepare for audits/inspections and manage project budgets
• Oversee administrative closeout procedures and ensure project documentation is archived
• Lead end-of-study meetings to document lessons learned
• Identify potential project risks and implement contingency plans
• Mitigate risks and keep clients informed throughout the study life cycle
• Contribute to SOP development and provide oversight and training to Associate PMs and Project Assistants

Requirements:

• 2 years of Project Management experience with Parexel or 3 to 5 years in related fields
• Experience as a Functional Team Leader or in coordinating clinical trials
• Knowledge of ICH-GCP and pharmaceutical industry regulations
• Proficiency in MS-Office products
• Bachelor's degree in a science-related field or equivalent work experience
• Advanced degree preferred
• Additional business degree or PMP certification is an advantage
• Scientific/Medical/Pharmacology background is an advantage