Project Manager, Early Phase

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

⚕️ Healthcare Insurance

🧬 Biotechnology

💊 Pharmaceuticals

💰 Venture Round on 1990-01

Healthcare Insurance • Biotechnology • Pharmaceuticals

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• 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. • 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 projects to completion within budget and schedule, ensuring contract specifications are met. • Monitor study timelines, recruitment, retention, and data cleaning. • Oversee administrative closeout procedures and ensure project documentation is archived. • Identify potential project risks and implement contingency plans.

🎯 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.

🏖️ Benefits

• Professional development • Remote work options