Parexel

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's Early Phase Clinical Unit in Glendale as a Clinical Research Nurse. Administer novel treatments and monitor participant safety in vital first-in-human trials. Requires an active CA RN license, 2+ years clinical experience, and BLS/ACLS certification. We offer competitive benefits, ...

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...

Join Parexel's Early Phase Clinical Unit in Glendale, CA as a Research Associate. Play a crucial role in Phase I trials, recruiting participants and conducting clinical visits. Requires a life science background, clinical/patient experience, and fluency in English and Mandarin. We offer extensive...

Join Parexel as a Senior Clinical Research Associate in the Paris Region. This role requires oncology trial experience and RECIST criteria knowledge. You will ensure protocol compliance and data integrity at investigator sites. We offer career growth, flexible work, and a patient-focused environm...

Seeking a Senior Clinical Research Associate (CRA) for a remote role in the UK. This position requires essential experience in oncology trials and RECIST criteria. You will ensure protocol compliance and patient safety while working on global projects. We offer flexible work arrangements, career ...

Join Parexel's global Project Leadership as a Clinical Trials Assistant in North Ryde, Sydney. You will support cross-functional teams to deliver patient-focused clinical trials, managing documents and communication throughout the trial lifecycle. This role offers a supportive, flexible environme...

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 in Warsaw as a Senior Statistical Programmer. Utilize your 5+ years of SAS programming and CDISC expertise to analyze clinical trial data across diverse therapeutic areas. Enjoy a fully flexible work arrangement, extensive training, and a supportive, inclusive environment focused on ...

Join Parexel in Taipei as a Statistical Programmer II. Utilize your SAS expertise to analyze clinical trial data, ensuring quality and compliance with ICH-GCP. This role offers growth through training, diverse therapeutic exposure, and flexible work arrangements in a supportive, global team envir...

Join Parexel's Early Phase Clinical Unit in Glendale, CA, as a Clinical Research Nurse. You will administer novel compounds and provide round-the-clock monitoring for volunteer participant safety in first-in-human trials. This role requires an active CA RN license, 2+ years of clinical experience...