Parexel
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
đź’Š Pharmaceuticals
đź’° Venture Round on 1990-01
Healthcare Insurance • Biotechnology • Pharmaceuticals
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.
Senior Clinical Research Associate, FSP
🔥 0 minutes ago
đź“Š Check your resume score for this job
Improve your chances of getting an interview by checking your resume score before you apply.
Parexel
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
đź’Š Pharmaceuticals
đź’° Venture Round on 1990-01
Healthcare Insurance • Biotechnology • Pharmaceuticals
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
• Contributes to the selection of potential investigators • Trains, supports, and advises Investigators and site staff in study related matters • Performs monitoring visits (remote and onsite) • Ensures data query resolution in a timely manner
🎯 Requirements
• Bachelor’s degree in related discipline, preferably in life science • Excellent knowledge of international guidelines ICH-GCP • Good medical knowledge and ability to learn relevant Client Therapeutic Areas • Basic understanding of the drug development process
🏖️ Benefits
• Health insurance • Flexible work arrangements • Professional development opportunities
Apply NowSimilar Jobs
đź•’ May 29
Clinical Research Associate conducting compliance assessments and monitoring across clinical trial sites for a leading pharma support organization. Managing documentation and ensuring data integrity in clinical studies.
🗣️🇫🇷 French Required
đź•’ May 29
Sr. Clinical Research Associate overseeing clinical trial sites and ensuring compliance with regulatory requirements at ICON. Managing site performance and collaborating with cross-functional teams.
🗣️🇫🇷 French Required
đź•’ May 5
Legal Research Analyst handling legal research and retrieval tasks for law firm clients. Requires strong research skills using various legal databases and tools.
đź•’ April 17
Worldwide Clinical Trials
1001 - 5000
🧬 Biotechnology
đź’Š Pharmaceuticals
⚕️ Healthcare Insurance
Clinical Research Associate managing oncology research projects at Worldwide Clinical Trials. Responsible for conducting research activities and ensuring compliance at participating sites with a focus on patient impact.
🗣️🇫🇷 French Required
đź•’ March 31
Manage clinical site monitoring services for multinational projects as Lead CRA. Responsible for design, oversight, and collaboration with stakeholders.
