Parexel
10,000+ employees
Founded 1983
đź’Ľ Consulting
🏥 Healthcare
📦 Logistics
đź’° 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.
Translational Medicine Scientist
🔥 0 minutes ago
🇺🇸 United States – Remote
⏰ Full Time
🟡 Mid-level
đźź Senior
🌎 Translator / Interpreter
🦅 H1B Visa Sponsor
đź‘» Ghost score 10%
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Parexel
10,000+ employees
Founded 1983
đź’Ľ Consulting
🏥 Healthcare
📦 Logistics
đź’° 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.
đź“‹ Description
• Review and interpret informed consent language for biospecimen and data use • Negotiate and manage genetic and biomarker consent requirements • Resolve complex consent and compliance questions with global stakeholders • Support high-impact clinical research and precision medicine initiatives • Partner with leading pharmaceutical and biotech organizations • Ensure biospecimens and patient data are used in accordance with participant consent
🎯 Requirements
• Bachelor's degree in a scientific field • 5+ years of experience with genetic and biomarker informed consents globally • Background in clinical trials, genetics, biomarkers, biobanking, or biospecimen management • Strong analytical, communication, and stakeholder management skills
🏖️ Benefits
• Health, Vision and Dental Insurance • Tuition Reimbursement • Vacation/Holiday/Sick Time • Flexible Spending and Health Savings Accounts • 401(k) with Company match • Pet Insurance
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