
10,000+ employees
Founded 1983
💼 Consulting
🏥 Healthcare
📦 Logistics
💰 Venture Round on 1990-01
Consulting • Healthcare • Logistics
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.
🔥 1 minute ago
🏄 California, Colorado, +1 more states – Remote
💵 $110k - $135k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research
🦅 H1B Visa Sponsor
👻 Ghost score 0%
Where this job comes from
Posted on Parexel's careers page, not through a job board
First seen by Remote Rocketship 1 minute ago

10,000+ employees
Founded 1983
💼 Consulting
🏥 Healthcare
📦 Logistics
💰 Venture Round on 1990-01
Consulting • Healthcare • Logistics
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.
• Own the sponsor relationship and serve as the central point of contact and escalation • Communicate project progress, risks, and solutions • Lead sponsor and project team meetings • Contribute to pre-award strategy, project management strategies, Bid Defense, and handover meetings • Lead study start-up activities, including site selection, contract and budget review, team and system setup, and IRB/EC and regulatory authority approvals • Direct internal and sponsor kick-off meetings • Lead clinical trials or programs through completion within budget and schedule • Monitor study timelines, recruitment, retention, data cleaning, project performance, and CTMS tracking • Manage project financials, including budgets, revenue recognition, milestone payments, and pass-through invoices • Prepare projects for audits and inspections • Oversee administrative closeout and document archiving • Lead end-of-study lessons learned meetings • Identify risks, develop contingency plans, and mitigate issues throughout the study life cycle • Contribute to SOP development • Provide oversight and training to Associate Project Managers and Project Assistants
• Bachelor's degree in a science-related field • 2 years of Project Management experience with Parexel or 3 to 5 years of experience in related fields • Early phase experience; site level experience is highly preferred • Experience as a Functional Team Leader or in coordinating clinical trials • Knowledge of ICH-GCP and pharmaceutical industry regulations • Proficiency in Microsoft Office products • Ability to lead cross-functional Parexel and sponsor teams • Ability to manage priorities, risks, escalations, and solutions across the study life cycle • Experience managing project systems, operational metrics, contracts, budgets, and financial processes
• Health, Vision & Dental Insurance • Tuition Reimbursement • Vacation/Holiday/Sick Time • Flexible Spending & Health Savings Accounts • Work/Life Balance • 401(k) with Company match • Pet Insurance • Paid time off • Life insurance • Additional benefit offerings in accordance with applicable plans
Apply NowImprove your chances of getting an interview by checking your resume score before you apply.
🔥 3 minutes ago
Clinical Trial Manager overseeing site management, monitoring, compliance, and risk mitigation for Syneos Health’s biopharmaceutical research programs. Coordinating CRAs, central monitors, sites, clients, and study milestones.
🔥 5 minutes ago
Clinical Research Associate monitoring clinical sites and patient safety for BeOne, a company developing cancer medicines. Managing compliance, data quality, training, and study milestones.
🔥 4 hours ago
Remote Clinical Research Associate monitoring clinical trials for ICON’s sponsor partners. Ensuring protocol compliance, site performance, data integrity, and regulatory standards.
🔥 7 hours ago
Clinical Trial Manager overseeing study startup, compliance, recruitment, and site operations. Supporting a contract research organization client with budgets, regulatory submissions, and research staff leadership.
🔥 8 hours ago
Clinical Trial Manager overseeing feasibility, startup, compliance, budgets, and conduct of CRO-sponsored clinical studies. Leading research staff and coordinating Sponsors, CROs, regulators, and clinic teams.