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 Manager, Feasibility
Job not on LinkedIn
🔥 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
• Oversight of activities • Evaluate the intent of the study concept and make informed recommendations based on scientific review • Effectively communicate with key stakeholders through the initial viability/feasibility concept phase • Utilize tools (e.g. Medidata, Symphony) to generate data to satisfy feasibility/viability requests • Author reports to inform project teams of assessments • Collaborate with cross-functional teams to evaluate study concepts and deliver comprehensive feasibility reports
🎯 Requirements
• Minimum 5 years of relevant experience • Excellent knowledge of GCP and regulations • Scientific understanding for the areas of interest for the client to help support effective viability considerations • Ability to author scientific documentation to support viability consideration. • Utilization of software applications to support data collection and clear interpretation of this data to assist in the evaluation of the study viability. • Experience of team management
🏖️ Benefits
• Complies with required training curriculum • Completes timesheets accurately as required • Submits expense reports as required • Updates CV as required
Apply NowSimilar Jobs
🔥 2 hours ago
Director, Clinical Scientist at Spyre Therapeutics designing and executing clinical trials for novel therapies in rheumatic diseases. Collaborating across functions to ensure robust study designs and high-quality data generation.
🇺🇸 United States – Remote
đź’µ $215k - $230k / year
⏰ Full Time
🟡 Mid-level
đźź Senior
🧪 Clinical Research
🔥 23 hours ago
Manager, Clinical Research Monitoring with Edwards improving patient lives through clinical evidence in cardiac innovation. Overseeing clinical trials and ensuring regulatory compliance for groundbreaking medical devices.
🇺🇸 United States – Remote
đź’µ $126k - $178k / year
⏰ Full Time
đźź Senior
đź”´ Lead
🧪 Clinical Research
🦅 H1B Visa Sponsor
đź•’ Yesterday
Clinical Trial Manager ensuring effective communication and compliance for site operations in oncology trials. Collaborating with stakeholders to meet recruitment and study objectives across trials in the US.
đź•’ Yesterday
Senior Clinical Trial Manager responsible for managing oncology trials and engaging with trial sites. Overseeing compliance, recruitment strategies, and trial management processes at ICON in the United States.
đź•’ Yesterday
Senior Clinical Trial Manager role managing trials in Immunology at ICON. Overseeing study operations and coordinating with local vendors for efficient execution.
