PSG Global Solutions Careers
Document Coordinator
PSG Global Solutions Careers, Cambridge, Massachusetts, us, 02140
Apply now and our proprietary system will quickly have you in front of a live recruiter.The OpportunityDescriptionWe're looking for a
Document Coordinator , working in
Pharmaceuticals and Medical Products
industry in
300 Third Street, Cambridge, Massachusetts, 02142, United States .
Maintains metrics for periodic reviewMakes updates in Veeva based on doc owner responseCommunicates with and assist end users understanding process and holding accountable to committed target datesSupports Veeva Vault Quality Docs
Our Client
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 skillsSOP writingTraining materials creation and delivery experienceeDMS use and administrative experienceProject management skillsAbility to work independently with minimal supervisionAble 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?
Document Coordinator , working in
Pharmaceuticals and Medical Products
industry in
300 Third Street, Cambridge, Massachusetts, 02142, United States .
Maintains metrics for periodic reviewMakes updates in Veeva based on doc owner responseCommunicates with and assist end users understanding process and holding accountable to committed target datesSupports Veeva Vault Quality Docs
Our Client
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 skillsSOP writingTraining materials creation and delivery experienceeDMS use and administrative experienceProject management skillsAbility to work independently with minimal supervisionAble 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?