RemoteOtterRemoteOtterExplore 62 Remote Ich Guidelines Jobs
Eurofins
Join Eurofins bioskin as a Data Manager to oversee data management in clinical trials.
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JPN - 2780 TPC
The Senior Manager, Clinical Partner Outsourcing ensures the effective execution of clinical studies through robust supplier contracts and strategic commercial negotiations.
Deciphera Pharmaceuticals
The Associate Director, Regulatory CMC will lead and execute CMC regulatory activities for clinical drug development at Deciphera.
Precisionmedicinegroup
Join Precision for Medicine as a Clinical Project Manager to lead global clinical trials in Oncology.
AbbVie
Join AbbVie as a Principal Strategic Medical Writer to lead and create high-quality clinical and regulatory documents.
AbbVie
The Clinical Research Associate II will manage clinical trial sites, ensuring compliance and data integrity while supporting patient recruitment.
AbbVie
The Clinical Data Systems Lead will oversee the integration of clinical technologies and data management to enhance clinical trial outcomes at AbbVie.
Precision for Medicine
The Clinical Research Associate II will oversee clinical studies, ensuring compliance and quality while maintaining a positive work-life balance.
Synchron
Join Synchron as a Senior Clinical Research Associate and play a key role in advancing groundbreaking brain computer interface technology.
ClinChoice
Join ClinChoice as a Global Labeling Lead Consultant, providing strategic support in pharmaceutical labeling while working remotely.
ClinChoice
Join ClinChoice as a Global Labeling Lead Consultant to provide strategic support and ensure compliance in pharmaceutical labeling.
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Arcus Biosciences
The Manager, Safety Quality and Compliance will oversee processes and systems for safety and pharmacovigilance compliance, supporting regulatory inspections and process improvement.
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Parexel International
Join Parexel as a Senior Clinical Research Associate I to manage oncology clinical sites in the Paris region.
AbbVie
The Principal Strategic Medical Writer leads the writing of clinical and regulatory documents, ensuring alignment with project goals and compliance with regulations.
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Acadia Pharmaceuticals
The Director of Medical Writing will lead the preparation of clinical and regulatory documents to support product development.