Parexel - IT - Administration

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.

Lead cross-functional clinical trial teams in Bengaluru to deliver patient-focused studies and accelerate treatments to market. This role requires project management skills, a science degree, and strong English proficiency. Enjoy a supportive, flexible environment with diverse projects and clear ...

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 ...

Join our team in Serbia as a Central Monitor (FSP). 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 central monitoring and RBQM. You'll play a key role in risk identifica...

Join Parexel as a Medical Director - Ophthalmology, working remotely from the Czech Republic or Europe. Utilize your deep therapeutic expertise to provide medical monitoring and consult on global drug development programs. This role requires an Ophthalmology physician with industry or clinical tr...

Join Parexel's Global Medical Sciences team as a Medical Director - Ophthalmology. This remote role in Serbia requires a qualified physician with strong ophthalmology and clinical trial expertise. You will provide medical monitoring, consult on drug development, and lead client relationships. Enj...

Lead clinical trial operations from startup to closeout in the U.S. as a Study Operations Manager. This FSP role requires 5+ years of operational experience and a scientific degree. You will oversee country-level planning, manage CROs, and ensure strategic delivery.