Parexel - United States, Remote work

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 Parexel FSP as a fully remote Clinical Study Physician in Oncology. This critical global role requires an MD with at least 4 years of clinical experience and oncology expertise. You will provide medical oversight from trial design through reporting, ensuring protocol integrity and patient sa...

Lead complex medical publication programs as a Senior Publications Project Manager at Parexel. This full-time remote role requires 5+ years' experience, iEnvision proficiency, and strong project leadership. Drive impactful healthcare communications from the US or Canada within a collaborative, fl...

Lead our clinical data management for late-phase oncology trials. This role requires 7+ years of pharmaceutical/biotech data management experience, strong project oversight, and CDISC/ICH-GCP proficiency. You will develop risk strategies, ensure data quality, and collaborate with stakeholders. Id...

Join our global team as a Study Physician in Oncology. This critical role provides medical oversight for clinical trials from design to reporting. We seek a qualified physician with pharma/CRO experience and strong analytical skills. This is a US-based position within a collaborative, internation...

Join Parexel's global oncology team as a Medical Director. Utilize your US/Canada board certification to provide expert medical monitoring and safety oversight for cutting-edge cancer trials. This role offers the chance to impact novel therapies, including immuno-oncology, with some travel requir...

Seeking a remote Clinical Study Physician specializing in Oncology. This global role requires an MD with 4+ years of clinical experience and industry/CRO background. You will provide critical medical oversight from trial design to reporting. Enjoy flexible work arrangements and a focus on profess...