Parexel - United States, Research and Development, Remote work

Lead our US site partnerships as a Site Care Partner CRA at Parexel. You will drive site start-up, activation, and relationship management for global clinical trials. This role requires strong GCP knowledge, excellent communication skills, and a commitment to patient safety. Enjoy career growth, ...

Join Parexel Consulting as a Regulatory Affairs Consultant. Leverage your 4-6+ years of CMC regulatory experience to develop strategies for FDA/EMA submissions. Enjoy a fully remote role in the US with flexible work arrangements and global client exposure. Drive product approvals in a supportive,...

Launch your clinical research career with Parexel's APEX CRA program. This accelerated training role offers foundational experience in monitoring and site management on global projects. Enjoy a remote US position with comprehensive benefits, including ACRP membership and development programs. Ide...

Join Parexel's FSP team as a Clinical Research Associate. You will ensure patient safety and data integrity by monitoring global clinical trial sites. This role requires ICH-GCP expertise, strong site management skills, and the ability to travel. We offer flexible work arrangements, career develo...

Join Parexel as a Clinical Research Associate in the US Midwest/West. Utilize your ICH-GCP knowledge and oncology experience to monitor sites and ensure patient safety. Enjoy a supportive team, career growth, and flexible work arrangements on global therapeutic projects.

Join Parexel as a Senior Clinical Research Associate (CRA) and play an integral role in accelerating treatments to patients. This remote US position involves national/international travel to monitor sites, ensuring compliance with ICH-GCP and local regulations. You will work on global projects ac...

Join Parexel, a leading global CRO, as a Biomarker Consent Specialist. You will author, review, and negotiate genetic and biomarker language in clinical trial informed consents. This remote US role requires 5+ years of global trial experience and expertise in genetic consents. We offer comprehens...

Join Parexel as a Senior Clinical Research Associate (CRA) in the United States. You will ensure trial conduct and patient safety, monitoring sites with 60-80% travel. Requires 3+ years monitoring experience, ICH/GCP knowledge, and fluency in English. Work on global projects with career growth in...

Join Parexel as a Senior Clinical Research Associate (CRA) in the United States. You will monitor global clinical trial sites, ensuring patient safety and ICH-GCP compliance. This role offers career growth, flexible work arrangements, and exposure to diverse therapeutic areas. Excellent communica...

Join Parexel as a Clinical Research Associate in Oncology, managing global trials from site activation to database lock. This role requires 3+ years of monitoring experience, with 2 years in Oncology, and fluency in English. You will ensure GCP compliance, travel 60-80%, and enjoy flexible work a...