Documentation Requirements Jobs in Princeton, NJ
Documentation Requirements Jobs in Princeton, NJ

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I. General SummaryUnder general supervision identifies registers and maintains records of all cancer patients by utilizing the IMPAC-MRS system. Analyze registry data; disseminate information in accordance with professional ethics. Assure data quality work effectively and efficiently More...
Become a part of our caring community and help us put health firstDevelops plans implements analyzes and organizes clinical operations for a specific location managed.Conducts/delegates the assessment and reassessment of patients including updating of care plans and interpreting patie More...
The Lead Data Manager is responsible for all data management activities in assigned clinical trials under supervision.Acts as primary communication point for project teams and company departments regarding clinical data managementActs as primary communication point for clients/vendors More...
Job Description Summary: We are seeking a highly motivated and detail-oriented Treasury Analyst to join our Treasury team. The Treasury Analyst will play a key role in supporting the Treasury team and managing various treasury functions including daily funding intercompany funding pay More...
Technical Project ManagerDuties: Manage technical implementation through design development and deployment of business intelligence (BI) Data Science (DS) and Data Engineering (DE) projects. Provide guidance for a diverse team of BI Engineers Data Engineers and Data Scientists. More...
Senior Manager, Global Regulatory Affairs, Strategy
At Genmab we are dedicated to building extranotordinary futures together by developing antibody products and groundbreaking knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create champion and maintain More...
We are seeking a dynamic and experienced Senior Manager or Director of Software Development to lead and scale our global software delivery organization. This strategic role oversees the entire software development lifecycle from planning to team leadership and project execut More...
The Lead Data Manager is responsible for all data management activities in assigned clinical trials under supervision.Acts as primary communication point for project teams and company departments regarding clinical data managementActs as primary communication point for clients/vendors More...
The Privia Coding & Provider Relations Specialist. will be accountable for providing ongoing support of the Privia services for enrolled Privia providers and their staff. The Privia Success Associate will serve as an integral member of the Privia program team responsible for More...
The Privia Coding & Provider Relations Specialist. will be accountable for providing ongoing support of the Privia services for enrolled Privia providers and their staff. The Privia Success Associate will serve as an integral member of the Privia program team responsible for More...
The Privia Implementation Manager plays a key role in the Privias provider innovation programs. They are responsible for the successful implementation of the Privia suite of products and services. These premium solutions remove burdensome tasks from providers to-do lists freeing them More...
Systech delivers digital product identification and traceability solutions that empower our customers with information to achieve compliance detect supply chain threats and gain transparency across the supply chain. Built on decades of experience as the leader in pharmaceutical serial More...
Changing lives. Building Careers.Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us change equals opportunity. Every day our colleagues are challenging whats possible and making headway to More...
You will be primarily responsible for maintaining and improving prelicensure curricula and all processes related to teaching/learning and assessment/evaluation to meet and exceed professional accreditation and regulatory standards based on the best available evidence. You will c More...
Associate Director Global Regulatory Affairs Strategy
At Genmab we are dedicated to building extranotordinary futures together by developing antibody products and groundbreaking knockyoursocksoff KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create champion and maintain a More...
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