Explore 47 Remote Ich Guidelines Jobs
The Medical Writer will provide clinical regulatory document support and ensure high-quality submissions in the bio-pharmaceutical industry.
The Senior Quality Auditor ensures compliance with regulations and provides oversight for quality and compliance activities in clinical studies.
Join AbbVie as a Bilingual Clinical Research Associate II, where you will monitor clinical studies and ensure compliance with regulatory standards.
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IMVT Corporation
The Senior Director, Medical Writing Portfolio Management, will oversee the production of high-quality regulatory documents for clinical submissions.
Join AbbVie as a Bilingual Clinical Research Associate II, responsible for overseeing clinical studies and ensuring compliance with regulatory standards.
Join AbbVie as a Bilingual Clinical Research Associate II to monitor and ensure compliance at clinical study sites.
Join AbbVie as a Clinical Research Associate I to support and manage clinical trials ensuring compliance with regulatory standards.
Biogen is seeking a Senior Clinical Trial Specialist to assist in executing clinical trials with minimal guidance while ensuring compliance with regulatory standards.
MMS
MMS
The Senior Medical Writer will write and edit clinical documents while ensuring compliance with regulatory standards.
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Regeneron Japan KK
The Director of Regulatory Labeling oversees the development and management of regulatory labeling processes for pharmaceutical products.
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BeiGene UK
The Clinical Research Associate is responsible for monitoring clinical trials and ensuring compliance with regulatory standards in the oncology field.
Join as an Associate Clinical Trial Lead, supporting clinical operations and site management for oncology trials.
Clinigen is seeking a Senior PV Project Manager to lead client programs and manage pharmacovigilance activities.
Join DELFI Diagnostics as a Principal Clinical Scientist to lead clinical studies and research collaborations aimed at improving cancer detection.
The Clinical Research Associate I role involves managing clinical trials and ensuring compliance while working remotely.