Jim Crumpley & Associates
New Jersey, New Jersey
Manager of Regulatory Affairs, BS degree and at least five years of generic drug RA experience to include ANDA filings. Ground floor opportunity with a major branded drug firm.
Responsibilities include:
Management of Generic regulatory activities t...
Source: CareersInPharmaceutical.com
Updated
8 days
1 hour
ago
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ImClone Systems Incorporated
Branchburg, New Jersey
MD with oncology experience in either academia or pharmaceutical industry with a strategic focus on scientific peer to peer interactions and research within the Medical Affairs department.
1. Clinical interface with ImClone inter...
Source: CareersInPharmaceutical.com
Updated
8 days
19 hours
ago
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Clinical Data, Inc.
New Haven, Connecticut
This position is part of the clinical development team and reports to the V.P. of Regulatory and Clinical Development. Responsible for managing the conduct of clinical trials and associated activities related to PGxHealth’s Phase III inve...
Source: CareersInPharmaceutical.com
Updated
14 days
ago
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Caraco Pharmaceutical Laboratories, Ltd.
Detroit, Michigan
Regulatory Affairs Asst Manager
Wixom, MI
Duration: Full Time
Job Description
Provides assistance to the Director/Sr. Manager of Regulatory Affairs in maintaining the daily operations...
Source: CareersInPharmaceutical.com
Updated
23 days
1 hour
ago
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Caraco Pharmaceutical Laboratories, Ltd.
Detroit, Michigan
Regulatory Affairs Sr Associate
Detroit, MI
Duration: Full Time
Job Description
Will prepare, review and submit labeling for various applications, i.e., Original ANDA’s, amendment...
Source: CareersInPharmaceutical.com
Updated
23 days
1 hour
ago
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Medpace
Cincinnati, Ohio
Position Type: Full-time
Medpace is a global contract research organization (CRO), based in Cincinnati, OH, that manages the clinical trial process for pharmaceutical and biotechnology companies. We are currently seeking a Regulatory Su...
Source: CareersInPharmaceutical.com
Updated
57 days
18 hours
ago
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