To provide assistance in support of clinical research studies; assist with implementation and coordination of studies; participate in recruitment of study participants; perform behavioral or diagnostic testing; assist with collection maintenance & reporting of clinical research data. ...
As a Clinical Trial Assistant you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Services/deliverables include the management of all documents and logistical and administrative tasks related to trial feasibility, start-up,...
Must maintain clinical practice as defined by state licensure, AANP and/or ANCC. ...
Must maintain clinical practice as defined by state licensure, AANP and/or ANCC. ...
The role of Assistant Professor includes teaching courses within a programmatic core discipline as assigned, acting as a Dissertation Chair and/or acting as a Dissertation Committee Member. Assistant Professor will email/record and post a welcome letter to their assigned students one week prior to t...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...
As a Clinical Trials Associate, you are responsible for providing administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects with Project Delivery services are performed timely and accurately. What the Clinical Trial Associate does. Assist proj...
Stanford GSB researchers are seeking assistance in gathering historical data on water pricing, conservation reminders, and rebates from the websites of approximately 200 California water agencies. The collected data will be inputted into a pre-formatted Google Sheet, following detailed instructions ...
Clinical Research Associate II. Verifies issues or risks associated with blinded or randomized information related to IP. May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. For Real World Late Phase, the CRA II will use the business card titl...
Collaborate with fellow research assistants, faculty, and other stakeholders to ensure the success of research projects. Research skills: Familiarity with research methodologies and tools. Conduct comprehensive literature reviews related to the assigned research projects. Summarize relevant findings...
Responsible for the development and design of improved administrative procedures to promote the timely processing and submission of all administrative deliverables. Performs a variety of administrative and office support duties. Positions may serve as the primary staff assistant to a department or m...
Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review and ongoing risk assessment to ensure quality standards and address concerns associated with study delivery at sites within established protocols and portfolio under gene...
The Clinical Care Coordinator is expected to communicate with the Kindred at Home clinical team and help facilitate timely patient follow-up for patients in need of (additional) services when appropriate. The Clinical Care Coordinator helps to ensure optimal continuity of care for patients transitio...
Job Title: Work-from-Home Research Travel Assistant Location: Remote Responsibilities: Coordinate travel arrangements for clients, including flights, accommodations, transportation, and activities. ...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Associate Director, Project Management. ...
Avesis is seeking a Senior Clinical UM/AG Audit Coordinator to review external regulatory and partner audits and corresponding corrective action plans. The Senior Clinical Audit Coordinator will also work closely with Operations management to rectify infractions as they are noted. ...
Our team of experts – nurses, physicians, psychologists, economists, sociologists, data scientists, and public health experts – advance evidence and save lives by leading rigorous research and evaluation; results-driven technical assistance and training; and leading-edge data science and technology ...
Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review and ongoing risk assessment to ensure quality standards and address concerns associated with study delivery at sites within established protocols and portfolio under gene...
The Procurement Associate will handle the important administrative compliance functions of Data Entry, Database Management, Electronic Email-box Management, and Federal, State & Local Reporting Requirements in various AIR and government systems. Established in 1946, with headquarters in Arlington, V...
You will report to the Trauma and Injury Prevention Clinical Director, IDOH Division of Trauma and Injury Prevention. Advanced knowledge of current developments in public health and in a special clinical area. ...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...
Position: Work-From-Home Research Travel Assistant Location: Remote Job Type: Full-time About HappyGo Travel Services: HappyGo Travel Services is a leading travel agency specializing in personalized travel experiences for clients worldwide. ...
Assists management team by mentoring other Clinical Research Associates. Assists with preparation and/or delivery of presentations for UBC Clinical Research Associate training, departmental training and/or sponsor specific training. At UBC, we provide services to enhance the entire drug development ...
The Clinical Research Associate is responsible for the identification, qualification, management and monitoring of clinical study sites and reference laboratories to support Meridian Bioscience clinical development programs. At least 2 years of clinical research experience; working for a sponsor org...
The Froedtert & the Medical College of Wisconsin regional health network is a partnership between Froedtert Health and the Medical College of Wisconsin supporting a shared mission of patient care, innovation, medical research and education. This position is responsible for engaging in patient educat...