Clinical Project Manager – Early Phase Trials

🔥 12 hours ago

🏄 California, Colorado, +1 more states – Remote

🏄 California – Remote ⛰️ Colorado – Remote 🤠 Texas – Remote

💵 $125k - $138k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🏥 Clinical Operations

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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

• Lead Parexel and Sponsor teams by leveraging clinical research experience and project management skills to develop tailored solutions for sponsors • Ensure operational excellence and successful execution of clinical operations and logistical strategies for EP clinical trials or programs • Manage the financial aspects of projects, including revenue recognition, milestone payments, and monthly pass-through invoices • Own the sponsor relationship and manage sponsor communication • Manage study start-up activities and ensure best practices are implemented • Monitor study timelines, recruitment, retention, and data cleaning • Oversee administrative closeout procedures and ensure project documentation is archived

🎯 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

• health insurance • 401k match • paid time off • annual performance-based bonus plan • annual salary review • additional total rewards incentives