Parexel - IT - Administration, Remote work

Seeking a Site and Monitoring Health Lead for the Northeast US. This site-facing FSP role ensures GCP compliance and CRO oversight for multinational clinical trials. Requires significant CRO monitoring oversight, Lead CRA experience, and up to 50% travel. Join a team dedicated to inspection-ready...

Senior Regulatory Affairs Associate sought for Parexel Consulting to lead radiopharmaceutical lifecycle management. Leverage expertise in CMC authoring, safety labelling, and Health Authority submissions. This remote role based in India offers flexible work, global client exposure, and mentorship...

Join Parexel as a Site Activation Partner in Ontario, Canada. Leverage your 2+ years of Study Start Up experience to manage essential documents and investigator site initiation. Ensure regulatory compliance with ICH/GCP and FDA guidelines while coordinating global clinical trials. Advance your ca...

Global Study Manager II sought for FSP role in the UK. Lead global clinical trials from strategy to database release, ensuring quality oversight and inspection readiness. Requires a Bachelor’s degree with 7+ years of operational trial experience, deep knowledge of GCP and study management. Drive ...

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.

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 our team as a Central Monitor in Romania. You will ensure clinical trial data quality and oversight using risk-based monitoring and data analytics. The role requires 5+ years of pharma/CRO experience and expertise in RBQM and central monitoring. You'll play a key role in risk identification ...