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Parexel - United States

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Biomarker Consent Specialist

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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...
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United States
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Not provided
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Biomedical Engineering Technologist

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Join Parexel in Glendale, CA, as a Biomedical Engineering Technologist. You will maintain, calibrate, and troubleshoot medical devices to ensure patient safety and support clinical trials. The role requires 2+ years of medical device experience, strong problem-solving skills, and a collaborative ...
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United States , Glendale, California
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30.00 - 34.00 USD / Hour
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Clinical Study Physician - Oncology

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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...
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United States , Remote
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Not provided
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Data Management Lead

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Join Parexel in San Francisco as a Data Management Lead, driving late-phase oncology and medical affairs projects. You will leverage your 7+ years of clinical data management expertise to ensure high-quality, compliant data delivery. This role offers a competitive benefits package and the chance ...
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United States , San Francisco
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99000.00 - 180000.00 USD / Year
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Financial Analyst Intern

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Launch your finance career with this Financial Analyst Internship in Raleigh. Gain hands-on experience in project economics, profitability drivers, and financial modeling while supporting Project Leaders. This role is ideal for current Finance/Accounting students seeking to apply their analytical...
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United States , Raleigh
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Not provided
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Senior Publications Project Manager

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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...
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United States
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Data Management Lead

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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...
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United States
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Not provided
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Study Physician - Oncology - FSP

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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...
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United States
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Not provided
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Medical Director, Oncology

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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...
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United States
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Not provided
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Clinical Study Physician - Oncology - FSP

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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...
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United States , Remote
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Senior Medical Writer - FSP

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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...
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United States
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Manager, Central Monitoring, Data Analysis - FSP

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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...
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United States
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Not provided
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