
10,000+ employees
Founded 1983
đŒ Consulting
đ„ Healthcare
đŠ Logistics
đ° Venture Round on 1990-01
Consulting âą Healthcare âą 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
đŒ Consulting
đ„ Healthcare
đŠ Logistics
đ° Venture Round on 1990-01
Consulting âą Healthcare âą 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.
âą Leads operational activities related to study planning, study execution, and the summarization of results from observational research studies âą Coordinates the end-to-end process for executing observational or non-interventional research studies in compliance with GPP and SOPs âą Plans, initiates, executes, and closes out primary data collection, chart review, database, and molecular epidemiology studies âą Collaborates with colleagues in GMSA to support lead scientists in overall operational support for study conduct âą Provides study-level management support including the execution of appropriate services for approved proposals/scopes of work âą Participates in protocol and interim/final report preparation and literature review abstraction
âą Two or more years of work experience within clinical/observational research or equivalent experience âą Oncology experience is required âą Excellent communication and interpersonal skills âą Basic knowledge of epidemiologic or outcomes research âą Fluency in English (written and spoken) âą Strong project management and prioritization skills âą Bachelor's degree in public health or science discipline
âą Professional development opportunities âą Flexible working arrangements
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