
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.
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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.
• Develop and maintain peer-to-peer relationships with key opinion leaders, principal investigators, sub-investigators, and healthcare providers within oncology clinical research • Lead site and patient engagement initiatives to improve operational excellence, trial performance, patient experience, and diversity and inclusion within clinical studies • Partner with cross-functional stakeholders to establish and achieve clinical operations objectives, work plans, recruitment timelines, and study deliverables • Develop and execute territory plans aligned with broader site engagement strategies • Identify, communicate, and share clinical research insights and emerging issues from research sites and healthcare providers with study teams • Support clinical study education activities for healthcare professionals and community stakeholders around clinical trial sites • Deliver scientific presentations and provide clinical information in response to unsolicited requests within academic, community, and healthcare settings, as appropriate • Maintain current expertise in oncology, relevant research trends, disease management practices, and the competitive landscape • Collaborate with internal and external stakeholders to strengthen site engagement strategies and enhance patient outcomes in clinical trials • Support study-related materials, advisory activities, medical congress engagements, and training initiatives while ensuring compliance with applicable regulations and company standards
• Advanced degree (PharmD, MD, PhD, or equivalent) with a minimum of 3 years of experience in oncology medicine, OR license as an RN, NP, CNP, PA, or equivalent with a Master's degree (or equivalent) and a minimum of 5 years of experience in oncology medicine • Minimum of 2 years of experience as a Medical Science Liaison or in a comparable industry or clinical role • Knowledge of ICH-GCP, regulatory requirements, and clinical trial processes • Demonstrated ability to analyse and communicate complex scientific and medical information to a variety of audiences • Strong communication, presentation, organizational, negotiation, and problem-solving skills • Excellent command of spoken English • Valid driver's license and ability to travel approximately 60% of the time • Experience working in clinical research, oncology, healthcare, or another regulated environment • Ability to collaborate across functions and build trusted relationships with healthcare professionals and research sites • Comfort working with digital platforms, scientific data, and clinical research processes • Experience in solid tumors, targeted therapies, or related oncology specialties • Strong understanding of healthcare systems, clinical practice trends, and oncology research environments • Established credibility and success in developing relationships with external experts and opinion leaders • Familiarity with field-based medical, scientific, or clinical engagement activities • Experience supporting clinical research programs within oncology therapeutic areas
• Medical Plan • Life Assurance • Pension • Comprehensive benefits package for eligible employees • Flexibility • Growth opportunities
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