We're looking for a Documentation Coordinator III, working in the Pharmaceuticals & Medical Products industry in Bridgewater, New Jersey, United States.
Ensures the security, accessibility, and proper distribution of R&D documents
Maintains multiple R&D documents and document management systems
Manages R&D documentation through the document Life Cycle
Retrieves and send electronic Documents as requested.
We're offering Competitive Compensation and Benefits. This position may present an opportunity to go permanent.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years’ experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
HS Degree or equivalent. An Associate or Bachelors degree is preferred.
3-5 years of experience working in a documentation control environment
Knowledge of electronic document control systems
Previous experience to include medical device/pharmaceutical regulated companies
Proficient in the use of Adobe and MS Office (Word/Excel/PowerPoint), copiers and scanners
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.