- Creates project work plans and work with manager to meet required timelines
- Manages day-to-day operational aspects of project
- Prepares for external management reviews
- Ensures project documents are complete, current, and stored appropriately
- Provides regular status updates to manager
- Resolves and/or escalates issues in a timely fashion
- Suggests areas for improvement along with possible solutions
- Collection and maintenance of questionnaires
- Data Entry
- Conduct worldcheck/D&B (if deemed necessary)
- Internet searches
- This is not an exhaustive, comprehensive listing of job functions. May perform other duties as assigned by the Vice President of HCC&P
- Location: U.S. compliance operations hub (NJ); up to 10% travel may be required
REQUIREMENTS:
- Minimum of 5 years of experience in the pharmaceutical and/or medical device industries - Proficiency in document management, both physically and electronically
- Knowledge of advanced search techniques such as Boolean operators, and ability to construct logical relationships among search terms
- Experience with development and preparation of information packages
- Process-oriented, with sharp focus and attention to detail
- Ability to juggle multiple priorities
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