Clinical Scientist – FSP

🔥 18 hours 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, preparation of meeting materials, and protocol deviation management • Support a single study or multiple studies • Lead a study with limited scope, such as Survival Follow-up • Interact with internal and external stakeholders, including study sites and committees, in support of clinical study objectives • Complete required training curriculum • Complete timesheets accurately and on time • Submit expense reports as required • Update CV as required • Maintain working knowledge of and comply with Parexel processes, ICH-GCPs, and other applicable requirements

🎯 Requirements

• At least 2 years Pharmaceutical and/or clinical drug development experience in the last 5 years required • TA-specific experience required for postings in Oncology IDV and GSM preferred • Indication specific experience preferred • Experience reviewing and resolving study related data issues, including issued queries, resolved queries, medical record review, and identifying data errors requiring clarification with study sites • Proficient in reviewing patient data and resolving discrepancies involving adverse events, adverse-event trends, endpoint management, and labs experience preferred • Demonstrated oral and written communication skills • Proficiency in Microsoft Office (Outlook, Word, Excel and PowerPoint) required • OneNote experience preferred • Degree in Life Sciences • Bachelor of Science, Bachelor of Arts, Master of Science, or PhD