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Regulatory Submissionsの求人-諏訪郡下諏訪町 - 29 Job Positions Available

29 / 21 - 26 求人
IQVIA 求人

Job Description SummaryJob Overview With global impact and oversight, manage a department of Biostatistics and Statistical Programming staff ensuring that target productivity (project allocations, utilization, and output) levels are met. May fulfill the role of site

IQVIA  23時間前
EY 求人

At EY, you’ll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture and technology to become the best version of you. And we’re counting on your

EY  23時間前
Comfort Systems USA 求人

Job Description Summary -Ensures a controlled documentation system, record retention, and information services including electronic records retention processes in accordance with regulatory requirements. Ensures compliance to the requirements from regulatory agencies. Maintains the technical and non-technical documentation change

Comfort Systems USA  22時間前
Alexion Pharmaceuticals 求人

This is what you will do: The Senior Manager, Project Management is accountable for the generation and maintenance of program timeline for Japan local portion including Advisory Board meeting, internal governance endorsements, PMDA consultation, J-CTN, clinical

Alexion Pharmaceuticals  22時間前
Michael Page 求人

Take lead in medical writing activities in authoring clinical/regulatory documents as well as submission requirements to obtain product approval. Align with global business strategies for local requirements Client Details * One of the top global biopharmaceutical companies in

Michael Page  17時間前
Michael Page 求人

Be part of a critical member in the RA organization. Lead in RA development/strategy activities to obtain product approval for various unmet medical needs. Client Details * Global leading pharmaceutical business specialising in womens health *

Michael Page  17時間前

新しい機会を逃さないで!

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regulatory submissions 求人 全国 諏訪郡下諏訪町

次も興味があるかもしれません:

Japanese

Drug Development

Clinical Trials

Biotechnology

Regulatory Affairs

Medical Devices

Risk Management

Regulatory Filings

Product Development

Briefing

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