In collaboration with investigators, responsible for tracking and completing protocol feasibility questionnaires. Coordinates Critical Document Collection to facilitate the timely opening of trials at the site. Communicates and collaborates with central operations and data management to identify and resolve any regulatory issues. Maintains Protocol Regulatory Documents in

Join us and grow your career with a certified Great Place to Work for the last eight years running. We are a team of Engineers, Architects, Surveyors and Scientists committed to making meaningful contributions to the world around us. Our quest for excellence goes beyond the ordinary; we seek extraordinary people who want to showcase their talents and join us in making a d

Requisition ID 31365 At Terumo Blood and Cell Technologies, our 7,000+ global associates proud to come to work each day, knowing that what we do impacts the lives of patients around the world. We make medical devices and related products that are used to collect, separate, manufacture and process various components of blood and cells. With our innovative technologies and

A. HMIS System Oversight and Support Provide technical assistance (group and individual user consultation) and data entry oversight to HMIS end users to enhance data quality and program performance. Collaborate and coordinate with program staff on HMIS program set up, data entry, analysis, and reporting. Promote the use of HMIS and reporting accountability throughout DMSS

McKesson is an impact driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and services that make quality care more accessible and affordable. Here, we focus on the health, happiness, and well being of you and those we serve we care. What you do at McKesson matters. We foster a culture where you can

As Director of Safety & Mission Assurance (S&MA), you will be responsible for the overall direction and implementation of all S&MA disciplines, ensuring consistency with corporate strategy, consistency of process across programs and projects, and customer satisfaction with the products and services provided. S&MA disciplines include Systems Safety, Reliability Engineering,

What Success Looks Like In This Job This position is responsible for ensuring appraisal processes have been completed through every step. Appraisers are assigned several work tasks for appeals and permits. This position will ensure that the process has accurately been completed as defined in the Assessor's Office procedures. This position will also ensure that every parce

include but are not limited to Design, Implement, and improve engineering and program Lifecyle management policies, procedures, and standards to be used for Test and Flight Operations systems. Manage data in Blue Origin eco system Establish effective communication with major stakeholders. Lead and/or support change control meetings to ensure risks and change impacts are we

Do you have the skills, expertise and passion that it takes to be a top notch quality engineer? Join our team and take your career to new heights! As a Quality Engineer II, you'll ensure all quality standards are met for our products and production equipment. You'll participate in the designing and testing of our processes, mechanisms, and equipment, and development of sta

Drive technology transactions, including negotiating and drafting cloud computing, software licensing, IT professional services, and other IT related supplier agreements. Facilitate the coordination of input from various subject matter experts throughout the negotiation process. Provide strategic advice and guidance to internal business teams regarding legal and business

Maintain a high standard of customer service by keeping up to date reporting and tracking procedures Follow the Quality Systems requirements for record keeping to ensure accuracy of reporting and for both internal and external customers Constant Monitoring and improvement of our ISO Certification and documenting procedures Help to develop & maintain Standardized Work Inst

Serve as legal regulatory counsel and strategic partner to DaVita Labs, with a primary emphasis on healthcare laws and regulations, as well as support for payor relations and contracting. In partnership with other DaVita attorneys and compliance teammates, assist business clients in identifying and resolving legal/regulatory matters related to business initiatives. Advise

Support Credentialing Team who is responsible for reviewing all applications submitted by providers to DaVita to be credentialed in our facilities. Identify and opine on elements that may be associated with increased risk to DaVita. Assist in updating medical staff bylaws. Provide legal guidance related to peer review investigations. Develop policies and process related t

Provide legal counsel on a variety of health care, corporate, and commercial matters arising in the day to day operations of DaVita's Integrated Kidney Care (DaVita IKC) division. Structure, negotiate and provide legal oversight for business transactions. Assist and collaborate with other DaVita attorneys, compliance teammates, and business leaders in identifying and reso

Drafts, reviews, analyzes, and negotiates plan and provider templates, agreements, and memoranda and other legal documents. Coordinates, manages and provides strategic advice on the full spectrum of health plan, integrated care, and provider contracting issues for Payor Partnerships. Facilitate the coordination of input from various subject matter experts throughout the n