We are looking for a QA Document Coordinator, working in the Pharmaceuticals & Medical Products industry in Cambridge, Massachusetts, United States.
Maintains metrics for periodic review.
Makes updates in Veeva based on doc owner response
Communicates with and assist end users understanding process and holding accountable to committed target dates.
The pay range we are offering is 35 to 41 per hour. 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
Technical writing skills
Training materials creation and delivery experience
eDMS use and administrative experience
Project management skills
Ability to work independently with minimal supervision
Able to shift priorities and manage more than one project at a time
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.