Net-Temps.
February 23, 2012

Jobseekers: Sign In | Sign Up Recruiters
Pharmacovigilance Scientist Back to search
Contact Information:
Algomod Technologies
116 John St 14th fl
New York, NY 10038
View other jobs with this company
Contact: 
Phone: 
Fax: 
Beatrice Miles
(877) 711-8700
212-306-0191

Post an Active Resume for free, and get
entered to win an Apple iPad 2!
Ends 2/23/12
Win an Apple iPad 2
Share this job:
Bookmark and Share
   Apply Online    |    Save this job   

Reference Number:
10-07853

Job Description:
The PV Scientist assists and supports the medical and scientific functions within safety evaluations for assigned products. Such tasks include preparation and coordination of reviews of individual case safety reports as well as aggregate safety data. The PV scientist will also support Risk Management Plans by serving as a coordinator for the acquisition and preparation of data for review from multiple sources. Collect, and/or organize the data collected as part of Pharmacovigilance plan, RMP, product recalls and surveillance activities. Manage outsourced data collection, organization preparation with vendors as required. Support surveillance activities re vendors, consultants, and databases- assist with contracts, proposals and data sharing. Collation of draft reports, progress reports required for updating Health Agencies of RMP activities. Support Physicians, such as case series review, data review, draft reports. Assist in organizing or running searches of safety or regulatory databases. Provide support to related PV activities such as preparation of reports for surveillance supports and collating reports for review of product quality data, support of health hazard evaluations, scientific presentations etc. Participate in preparation, analysis and writing of ad-hoc and aggregate regulatory reports and, labeling support documents.

Experience Level:
1 Year

Requirements:
The Pharmacovigilance Scientist has an advanced academic degree biological or natural science or health-care discipline (e.g. MS, MPH, etc). Previous experience within the pharmaceutical industry and at least 1 year pf post-marketing safety data analysis preferred but not required. Familiarity with industry principles of drug safety, drug development, pharmacology, biostatistics, and pharmacoepidemiology. Basic knowledge of common data processing software. Excellent verbal and written communication skills. Ability to interpret, analyze and clearly present scientific and technical data in verbal and written . Functional knowledge of EXCEL, PowerPoint, Microsoft Word. Team player, ability to work under tight timelines with poise. Ability to thrive in a global, matrix environment. Ability to manage high workload and critical issues.

Location:
Horsham PA

Duration:
6 - 9 months

Pay Rate:

Similar Jobs
  Horsham, PA   Pharmacovigilance Scientist
  Fort Washington, PA   Device and Pharmacovigilance Alliance Manager
  Thousand Oaks, CA   Project Manager
  Bridgewater, NJ   Medical Writer
  Princeton, NJ   Data Analyst / Data Steward
  New York, NY   Drug Safety, Pharmacist, Nurse, Pharmacy

   Apply Online    |    Save this job   

Date Posted: 02/15/2012
Last Updated: 02/15/2012
Similar Job Searches
Pennsylvania Jobs
Scientific Jobs