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Listed below are the top 10 out of 56 listings that are in the same industry and location as the job you were looking for. To see more than 10 listings, click here to search similar jobs in Bridgewater, NJ
Job Summary: Interface with Spine international RA affiliates to: Plan, organize, and implement strategies and activities required to procure regulatory approval ...
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Plan, organize and implement strategies and activities required to procure regulatory approval for new and revised product lines. Ensure compliance with all ...
Yoh has a contract opportunity for a Senior Clinical Data Analyst (SAS) to join our client in the Park Ridge, NJ area. Job Responsibilities: Perform SAS programming ...
MedFocus Pharmaceutical Research Opportunities - Nutley, NJ US
COMPANY INFO: NOW HIRING!! Are you looking to expand your career and enhance your professional skills? MedFocus is now seeking a Clinical Research Data Manager ...
MedFocus Pharmaceutical Research Opportunities - Bridgewater, NJ US
COMPANY INFO: NOW HIRING!! Are you looking to expand your career and enhance your professional skills? MedFocus is now seeking a Drug Safety Assistant Our client ...
Smith Hanley Consulting Group is seeking a Drug Safety Associate for an opening in Hawthorne, NY. Position Overview: This position will be responsible for the ...
Senior Clinical Data Manager Florham Park, NJ Contract position Responsible for providing timely and professional ongoing quality management of clinical trial ...
REPORTING TO: Senior Data Manager LOCATION: Center for Biomedical Research, New York, NY JOBS SUPERVISED: N/A ASSIGNMENT LENGTH: Two years, renewable by mutual ...
For your reference, we have included the original job posting below.
Drug Safety Data Management Specialist
Job Number:
42993268
Company Name:
Sunrise Systems Inc
Job Location:
Bridgewater, NJ US
Job Category:
Science & Biotech
Drug Safety Data Management Specialist
Job description: ? Book-in and data enter information into the global safety database for initial or follow up cases received via paper, fax or email. Accept E2B cases received through the Argus Electronic Submissions Module (ESM) from license partners and other submitters as necessary. ? Monitor electronic mailboxes and Argus ESM to ensure timely acceptance of Adverse Event (AE) Reports Perform. ? Ensure proper coding of events and drugs for cases to ensure correct forwarding to the relevant Th...