Clinical Scientist – FSP

🕒 February 17

🇺🇸 United States – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 65%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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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 and scientific conduct of clinical studies • Provide adjudication support • 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, to support 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

• MS Office Suite experience, including Word, Excel, and PowerPoint • Advanced Excel skills, including pivot tables and VLOOKUPs • Proficient written and spoken English • Oncology experience required • Bachelor's, Master's, or PhD in Life Sciences with 2+ years of relevant career experience • If no degree in Life Sciences, Bachelor's degree with significant experience in clinical development (>5 years) • 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 consideration regardless of legally protected status • Willingness to travel as required for key company meetings