Clinical Research Associate

🔥 15 hours ago

🌵 Arizona – Remote

🌵 Arizona – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 10%

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Parexel

WebsiteLinkedInAll Job Openings

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.

📋 Description

• Manage clinical trial investigator sites, including site management, monitoring, and close-out • Ensure patient safety and quality study execution in accordance with applicable laws, GCP, and sponsor standards • Manage investigator site relationships and operational activities from site activation through database lock • Serve as primary contact for assigned investigator sites and coordinate with Site Care Partners, study teams, vendors, and site personnel • Provide site development, coaching, training, protocol training, and recruitment support • Conduct onsite and remote/electronic monitoring for site initiation, routine monitoring, and site closure • Monitor adverse events and serious adverse events and collaborate with the Drug Safety Unit • Submit TMF documentation, site reports, follow-up letters, protocol deviations, recruitment updates, clinical supply information, study progress, and metrics • Identify and resolve site issues; develop corrective and preventative actions • Resolve data queries and conduct investigator site close-out activities • Oversee investigational product receipt, handling, accounting, storage, and destruction • Support database release and, where appropriate, perform unblinded monitor responsibilities • Maintain product, protocol, and therapy-area knowledge and support patient safety and clinical guidance • Drive quality-event remediation and audit CAPA activities when applicable

🎯 Requirements

• Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations • Minimum 2 years relevant experience in clinical research site monitoring • Fluent in English and the native language(s) of the country they will work in • Ability to travel 60–80% • Valid driver’s license and passport required • Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background, or equivalent

🏖️ Benefits

• Equal opportunity employment consideration regardless of legally protected status • Travel allowance implied by role travel requirements (no specific compensation stated)