Parexel - United States, Remote work

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...

Join Parexel as a Senior Medical Writer in the US. Utilize your scientific expertise to author key clinical documents like protocols, study reports, and CTD summaries. This role requires strong writing skills, ICH-GCP knowledge, and collaboration within cross-functional teams. Benefit from a supp...

Lead centralized monitoring for global clinical trials as a Manager, Data Analysis. Configure and maintain RBQM systems, utilizing programming expertise in R, SQL, or SAS for advanced data analysis and KRI/KPI reporting. This US-based role requires 4+ years of pharma experience and direct RBQM sy...

Join Parexel as an Investigator Financial Analyst II in the United States. You will steer investigator budget management for crucial clinical projects, translating clinical conduct into financial impact. This role offers a collaborative environment, comprehensive benefits, and flexible working ho...

Join Parexel as a Regulatory CMC Project Manager. Utilize your 3+ years of CMC regulatory experience to manage complex submissions and strategic plans for biopharma clients. Enjoy a fully remote role with East Coast hours, career growth, and expert mentorship. Be part of a supportive team shaping...

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...

Lead global clinical trials as a Project Leader at Parexel's Biotech Division. This remote US role requires 2+ years of CRO/biotech experience managing cross-functional teams, budgets, and timelines. Enjoy a supportive, empowered environment with flexible work arrangements and diverse therapeutic...

Join Parexel Consulting as an Advanced Analytics Consultant, specializing in Meta-Analysis and HTA. Utilize your statistical expertise in R and GitLab to design evidence-generation plans and conduct network meta-analyses for global clients. This remote US role offers a dynamic team, career growth...