If you possess strong software development prowess in C, C++, and Python, are well-versed in debuggers like gdb, Valgrind, windbg, have a deep understanding of network protocols and inter-process communication, and have a knack for executing guided research tasks, we're eager to uncover your potenti...
The role of the Oncology Research Pre-Post Award Associate is to develop the clinical trial agreements, budgets and coverage analyses for industry-sponsored clinical trials that bring new treatment options to our patients; and complete research billing review in Epic; and facilitate research invoici...
Associate Cyber Applied Research Scientist (CH). If you possess strong software development prowess in C, C++, and Python, are well-versed in debuggers like gdb, Valgrind, windbg, have a deep understanding of network protocols and inter-process communication, and have a knack for executing guided re...
R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. ...
We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development as a Clinical Research Associate II assigned to Early Development trials (Phase I). ICON plc is a world-leading healthcare intell...
The Clinical Research Associate is the clinical sites’ direct point of contact and accountable for managing site quality and delivery from site identification through close-out. The Clinical Research Associate will oversee the conduct of the trial at designated sites, ensuring the rights and well-be...
If you possess strong software development prowess in C, C++, and Python, are well-versed in debuggers like gdb, Valgrind, windbg, have a deep understanding of network protocols and inter-process communication, and have a knack for executing guided research tasks, we're eager to uncover your potenti...
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 ...
A full-time Research Associate position is available in the lung pharmacology laboratory at Shreiber School of Veterinary Medicine, led by the Associate Dean for Research and Graduate Studies. A Carnegie-classified R2 (high research activity) institution, Rowan has been recognized as the fourth fast...
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. ...
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...
We are looking for a skilled and experienced, part time, temporary, Research Associate III who will be responsible for supporting our research activities including performing experiments and generating reliable data. The duties and responsibilities of the Research Associate III include the following...
Senior Clinical Research Associate. 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. ...
Works on multiple oncology trials.Quality of life focus wtih Regional Travel.Demonstrated leadership, through involvement in specific initiatives when needed, and/or SME to systems and/or processes • Mentors/coaches junior flex team.Acts as Lead SM-training other SMs on study.Develops site start up ...
This research associate position will have the opportunity to co-teach with an experienced clinician and to participate in supervision rounds and discussions of clinical pedagogy with clinical teaching fellows from Rutgers Newark and Seton Hall. The NJSBF Teaching Research Associate will co-teach in...
Works on multiple oncology trials.Quality of life focus wtih Regional Travel.Demonstrated leadership, through involvement in specific initiatives when needed, and/or SME to systems and/or processes • Mentors/coaches junior flex team.Acts as Lead SM-training other SMs on study.Develops site start up ...
The Early Clinical Development Senior Clinical Research Associate will have relevant Phase I experience, responsible for conducting monitoring activities for one or more client sponsored studies. Responsible for monitoring clinical trial quality and site management for client sponsored studies that ...
We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development as a Clinical Research Associate II. ICON plc is a world-leading healthcare intelligence and clinical research organization. ...
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 role of the Oncology Research Pre-Post Award Associate is to develop the clinical trial agreements, budgets and coverage analyses for industry sponsored clinical trials to bring new clinical trials to our patients and complete research billing review in Epic and facilitate research invoicing for...
As a Sr CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. ...
The Early Clinical Development Senior Clinical Research Associate will have relevant Phase I experience, responsible for conducting monitoring activities for one or more client sponsored studies. Responsible for monitoring clinical trial quality and site management for client sponsored studies that ...