Parexel - United States, Research and Development

Lead clinical operations for diabetes trials as a Senior Clinical Trial Manager in San Francisco. Oversee global teams, ensuring on-time, on-budget, and quality delivery. Requires substantial trial coordination experience and strong leadership skills. Build trusted partnerships with sponsors and ...

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 as a Senior Clinical Research Associate (CRA) and play a vital role in accelerating treatments to patients. You will monitor global clinical trial sites, ensuring compliance with ICH-GCP and local regulations. This US-based role offers career growth, flexible work arrangements, and e...

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 our clinical research team as a Clinical Scientist. You will support the scientific conduct of studies, including medical monitoring and protocol management. This role requires a Life Sciences degree or extensive clinical development experience, plus strong communication skills. It offers a ...

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 our client's team in Springhouse, PA as a Scientist III in Regulated Immunogenicity & Molecular Bioanalytics. This FSP role requires 3-5 years' experience executing molecular assays like qPCR/dPCR and NGS in a GxP environment. You will generate quality data, ensure compliance, and collaborat...

Join our team as a Scientist III - Analytical Chemist on the third shift in Rahway, NJ. This role requires hands-on experience with HPLC, GC, and wet chemistry methods within a cGMP environment. You will operate and maintain analytical instrumentation, ensuring high-quality, compliant results. We...

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...

Lead global clinical trials for Biotech clients at Parexel. This project leadership role requires 2+ years of CRO/Biotech experience managing cross-functional teams, budgets, and timelines. Enjoy a supportive, flexible environment with diverse therapeutic areas and clear career progression in the...