Clinical Research Associate – CRA II/Senior, Metabolic

🔥 0 minutes ago

🏈 Alabama, Arizona, +41 more states – Remote

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⏰ Full Time

🟠 Senior

🧪 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 sites from identification through closeout • Serve as the primary point of contact for assigned clinical sites • Conduct qualification, site initiation, monitoring, and termination visits at assigned clinical sites • Prepare timely visit and contact reports • Manage site quality and delivery • Address site questions and resolve issues • Oversee study integrity and build relationships with investigators and site staff • Review trial performance and safeguard study participants' rights, safety, and well-being • Develop patient recruitment strategies to support enrollment timelines • Ensure compliance with SOPs, study protocols and amendments, Good Clinical Practice, and regulatory requirements • Evaluate reported data quality and integrity, site performance, and investigational product accountability • Monitor regulatory documentation completeness and quality • Perform site document verification

🎯 Requirements

• At least 18 months of direct onsite monitoring experience as a Clinical Research Associate • Metabolic/MASH and/or Obesity clinical trial monitoring experience • Bachelor's degree or equivalent in biological science, pharmacy, or another health-related discipline • Knowledge of Good Clinical Practice, applicable regulatory requirements, and clinical trial processes • Experience using a Clinical Trial Management System, an Electronic Document Management System, and Microsoft Office applications, including Excel and Word • Strong site relationship management, problem-solving, communication, interpersonal, written, verbal, organizational, and attention-to-detail skills • Ability to work independently with urgency and limited oversight • Ability to manage multiple priorities, evaluate changing scenarios, apply study protocols, and meet project timelines • Ability to collaborate within a matrixed team and communicate clearly with internal and external stakeholders • Ethical, patient-focused approach • Ability to work in the United States

🏖️ Benefits

• 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 • Potential eligibility for additional incentives, bonuses, or other compensation programs