Parexel - United States, IT - Software Development

Join Parexel as a Clinical Research Associate (CRA) in Early Development Oncology, covering the Northeast US. Leverage your 3+ years of site monitoring experience and GCP/FDA expertise to oversee clinical trials from activation to database lock. Enjoy 60-80% travel, flexible work arrangements, an...

Senior Regulatory Consultant sought to lead global regulatory strategy and program management for biopharma clients. Leverage 7+ years of experience in regulatory affairs and submissions (IND/BLA/MAA) to drive product development. This remote role offers mentorship, diverse therapeutic exposure, ...

Join Parexel in Newton, MA, as a Principal Statistical Programmer. Lead statistical programming for clinical trials, ensuring compliance with CDISC and FDA regulations. Utilize advanced SAS programming to analyze data across diverse therapeutic areas. Benefit from career growth, flexible work, an...

Lead clinical sample logistics and data operations in this remote US role. Utilize your expertise in Python, R, or SQL to develop tracking tools and ensure data integrity for biomarker studies. This position requires strong programming skills and 6+ years of clinical research experience to stream...

Join Parexel as a Senior Medical Writer in the US. Utilize your scientific expertise to author key clinical documents like protocols, study reports, and CTD summaries. This role requires strong writing skills, ICH-GCP knowledge, and collaboration within cross-functional teams. Benefit from a supp...