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Merck
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West Point, Pennsylvania
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comprehensive understanding of global regulatory expectations and contribute to regulatory documents and ... to business operations, in which case you may not be offered employment, or your employment could be
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Merck
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Rahway, New Jersey
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comprehensive understanding of global regulatory expectations and contribute to regulatory documents and ... to business operations, in which case you may not be offered employment, or your employment could be
...
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Merck
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Boston, Massachusetts
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comprehensive understanding of global regulatory expectations and contribute to regulatory documents and ... to business operations, in which case you may not be offered employment, or your employment could be
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Merck
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San Francisco, California
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global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory ... )), and representing our team at regulatory meetings.
**Education Minimum Requirement
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Merck
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Boston, Massachusetts
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global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory ... )), and representing our team at regulatory meetings.
**Education Minimum Requirement
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Merck
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Upper Gwynedd, Pennsylvania
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global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory ... )), and representing our team at regulatory meetings.
**Education Minimum Requirement
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Merck
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Rahway, New Jersey
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global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory ... )), and representing our team at regulatory meetings.
**Education Minimum Requirement
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Merck
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Tallahassee, Florida
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
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Merck
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Denver, Colorado
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
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Merck
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Frankfort, Kentucky
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
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Merck
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Lansing, Michigan
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
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Merck
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Bismarck, North Dakota
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
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Merck
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Charleston, West Virginia
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
...
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Merck
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Santa Fe, New Mexico
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
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Merck
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Salem, Oregon
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
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Merck
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Augusta, Maine
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
...
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Merck
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Topeka, Kansas
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
...
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Merck
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Concord, New Hampshire
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
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Merck
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Jackson, Mississippi
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
...
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Merck
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Springfield, Illinois
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
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Merck
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Providence, Rhode Island
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
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Merck
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Des Moines, Iowa
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
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Merck
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Albany, New York
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
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Merck
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Montpelier, Vermont
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
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Merck
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Honolulu, Hawaii
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
...
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Merck
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Indianapolis, Indiana
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
...
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Merck
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San Francisco, California
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
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Merck
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Little Rock, Arkansas
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
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Merck
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Pierre, South Dakota
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
...
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Merck
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Annapolis, Maryland
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understanding of global regulatory expectations for small molecules and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial
...