Parexel
10,000+ employees
Founded 1983
âïž Healthcare Insurance
𧏠Biotechnology
đ Pharmaceuticals
đ° Venture Round on 1990-01
Healthcare Insurance âą Biotechnology âą 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.
Principal Medical Writer
đ May 21
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Parexel
10,000+ employees
Founded 1983
âïž Healthcare Insurance
𧏠Biotechnology
đ Pharmaceuticals
đ° Venture Round on 1990-01
Healthcare Insurance âą Biotechnology âą 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.
đ Description
âą Author Clinical Documents âą Gather, review, analyze, and evaluate pertinent resources for clinical documents âą Train self and provide guidance to others for medical writing âą Revise document drafts based on feedback âą Ensure all work is of high quality before distribution âą Operate as project lead writer/submission coordinator âą Manage contributions of multiple writers âą Develop, coordinate, and oversee work plans âą Monitor the progress of individual project tasks âą Build and maintain collaborative relationships with teams/clients
đŻ Requirements
âą Bachelor's degree in Life Sciences/Health Related Sciences or equivalent âą Demonstrated understanding of clinical research, drug development process, and applicable regulatory guidelines âą Broad experience in preparation of all types of clinical regulatory documentation âą Experience in management of complex medical writing projects âą Knowledge of resource management and productivity metric management âą Advanced word processing skills, including MS Office (expertise in Word) âą Ability to travel âą Fluent in written and spoken English.
đïž Benefits
âą Paid time off âą Flexible working hours âą Professional development opportunities
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