Clinical Scientist – FSP

🔥 0 minutes ago

🇺🇸 United States – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🦅 H1B Visa Sponsor

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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

• Assist the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies • Support adjudication activities • Support medical monitoring • Prepare imaging data reconciliation • Prepare meeting materials • Manage protocol deviations • Support a single study or multiple studies • Lead studies with limited scope, such as Survival Follow-up • Liaise with cross-functional lines • Interact with internal and external stakeholders, including study sites and committees, in support of clinical study objectives • Complete required training curriculum • Complete timesheets accurately • Submit expense reports • Update CV as required • Maintain working knowledge of and comply with Parexel processes, ICH-GCPs, and other applicable requirements

🎯 Requirements

• Oncology experience is required • Bachelor's, Master's, or PhD in Life Sciences with 2+ years of relevant career experience • If no degree in Life Sciences, a Bachelor's degree with significant experience in clinical development (>5 years) is required • Demonstrated oral and written communication skills • MS Office Suite experience required, including Word, Excel, and PowerPoint • Advanced Excel skills required, including pivot tables and VLOOKUPs • Proficient in written and spoken English • Experience with adjudication support, medical monitoring, imaging data reconciliation, preparation of meeting materials, and protocol deviation management • Pharmaceutical experience beneficial but not required • 2 years of medical monitoring experience preferred

🏖️ Benefits

• Equal opportunity employment • Willingness to travel as required for key company meetings