Clinical Scientist – FSP

🔥 4 minutes ago

🇺🇸 United States – 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

• Assist the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies • Support adjudication, medical monitoring, imaging data reconciliation, meeting-material preparation, and protocol deviation management • Support a single study or multiple studies • Lead a limited-scope study, 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 knowledge of and comply with Parexel processes, ICH-GCPs, and applicable requirements

🎯 Requirements

• Demonstrated oral and written communication skills • MS Office Suite experience required, including Word, Excel, and PowerPoint • Proficient in written and spoken English • Proficient in local language, as applicable • Willingness to travel as required for key company meetings • Pharmaceutical experience beneficial but not required • Therapeutic Area-specific experience beneficial • 2 years medical monitoring experience preferred • Bachelor's/Master's/PhD in Life Sciences with 2+ years relevant career experience • If no degree in Life Sciences, significant experience in clinical development (>5 years)

🏖️ Benefits

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