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Parexel International Limited is a leading global biopharmaceutical services organization headquartered near Boston, Massachusetts, and in Durham, North Carolina. With over 16,000 employees and a presence in more than 100 countries, Parexel specializes in comprehensive drug development capabilities, including regulatory expertise, Phase I-IV clinical research services, and advanced commercialization solutions. The company is dedicated to improving global health by providing innovative clinical development solutions, underpinned by a strong commitment to empathy and making a difference in patients' lives. Parexel's collaborative approach fosters partnerships across various disciplines, ensuring high-quality scientific contributions and the successful delivery of epidemiology services and real-world studies.
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Parexel International
Join Parexel as a Clinical Data Analyst I/II and contribute to clinical data cleaning and management in a global healthcare environment.
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Parexel International
The Regulatory Affairs Consultant is responsible for developing CMC strategies and managing regulatory submissions to ensure compliance with health authority guidelines.
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Parexel International
The Senior Clinical Research Associate is responsible for managing clinical studies and ensuring compliance with guidelines while collaborating with local teams.
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Parexel International
The Senior Regulatory Affairs Associate is responsible for managing life cycle maintenance and regulatory submissions across various international markets.
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Parexel International
Join Parexel as a Senior Statistical Programmer to enhance patient-reported outcomes in oncology through SAS programming.
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Parexel International
Join Parexel as a Senior Clinical Research Associate I to manage oncology clinical sites in the Paris region.
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Parexel International
The Principal Statistical Programmer leads statistical programming efforts to support clinical trials at Parexel, ensuring high-quality deliverables and compliance with regulatory standards.
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Parexel International
The Senior Regulatory Affairs Associate will manage regulatory submissions and compliance for drug products, ensuring adherence to global standards.
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Parexel International
The Senior Statistical Programmer at Parexel is responsible for leading statistical programming projects, ensuring quality and compliance in clinical trials.
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Parexel International
Join Parexel as a Senior Data Engineer to lead data management solutions for clinical trials, ensuring high-quality deliverables and project success.
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Parexel International
The Senior Clinical Research Associate is responsible for managing clinical studies and ensuring compliance with regulations while collaborating with study teams.
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Parexel International
The Study Operations Manager I oversees clinical study management and ensures compliance with regulatory standards while leading local study teams.
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Parexel International
Join Parexel as a Software Engineer to develop impactful software solutions in the healthcare sector.
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Parexel International
The Site Care Partner is responsible for managing clinical trial sites and ensuring operational success throughout the study lifecycle.
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Parexel International
The Senior IT Auditor will manage IT risks through audits, ensuring compliance with standards and regulations while contributing to global health initiatives.