Parexel - Remote work

Senior Data Engineer role in Taiwan focused on creating standardized, customizable data visualizations for clinical trial decision-making. Requires 1-3 years of experience, proficiency in R Shiny, Git, and tidyverse, plus a basic understanding of clinical data structures. You will support study t...

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, ...

Parexel FSP seeks a Country Study Operations Manager I in Mexico or Argentina. You need a Bachelor's degree with 5+ years of clinical trial experience, or a Master's with 3+ years. Lead local study teams, manage country-level plans, and support global trials. This role offers the chance to drive ...

The Real-time Visual Analytics Specialist designs interactive data visualizations for Medical Data Review and safety signal detection in Taiwan. This role requires 1-3 years of experience with R Shiny, Git, and tidyverse, plus a Bachelor’s in life sciences or data science. You will support RBQM p...

Lead global clinical trials for biotech clients in this remote US role. Utilize your project management expertise within a CRO or pharma setting to deliver patient-focused studies. Drive operational excellence while enjoying a supportive, flexible environment with diverse therapeutic challenges.

Lead the development of global processes and procedural documentation for clinical, medical, safety, and regulatory functions. This role requires 5-8 years of pharmaceutical process design experience and expertise in quality management systems. You will manage a matrix team and projects, ensuring...

Join Parexel, a leading global CRO, as a Clinical Operations Assistant. Support CRAs and project teams with administrative tasks, site payments, and trial master file management in this remote Mexico role. Requires a healthcare/science degree, English fluency, and site experience. Contribute to l...

Lead the development of global processes and procedural documentation (SOPs, policies) for a major sponsor's clinical, medical, and safety organizations. This senior remote role in Argentina, Brazil, or Mexico requires 5-8 years of pharmaceutical process design experience. You will manage complex...

Lead our Site and Monitoring Health team, ensuring clinical trial quality and CRO oversight. This site-facing role requires significant monitoring and lead CRA experience, with up to 50% travel. Apply your expertise in GCP, risk-based oversight, and innovative problem-solving within a US-based FS...

Lead global clinical trials as a Senior Manager in this fully remote role based in Italy or the UK. You will provide end-to-end operational leadership, ensuring on-time and compliant delivery. Essential requirements include 7+ years of global trial management and CRO oversight experience. Drive s...

Join Parexel Consulting as a Senior Regulatory Affairs Consultant specializing in Regulatory Intelligence. Utilize your 5-7 years of experience to provide strategic intelligence, helping biopharma and device clients navigate FDA and global regulations. This remote US role offers flexible work, ca...

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...