- Mitsubishi Chemical Group (Jersey City, NJ)
- …+ Identifies and implements innovative solutions to resolve roadblocks in patient recruitment and clinical trial execution via development of an overall ... in vendor management, leading CROs/various contracted resources, site monitoring and clinical quality compliance, andmanaging clinical trial budgets… more
- Regeneron Pharmaceuticals (Armonk, NY)
- …etc. + Oversees set-up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS), Trial Master File (TMF) etc. + ... Ensures compliance with the clinical trial registry requirements + Identifies outsourcing...+ Leads the development of and oversees implementation of patient recruitment and retention strategies and acts… more
- Regeneron Pharmaceuticals (Armonk, NY)
- …etc. + Oversees set-up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS), Trial Master File (TMF) etc. + ... Ensures compliance with the clinical trial registry requirements + Identifies outsourcing...+ Leads the development of and oversees implementation of patient recruitment and retention strategies and acts… more
- New York University (New York, NY)
- …living with HIV (PLWH). The project will test an intervention to directly target patient barriers to quitting and clinical care barriers to tobacco treatment by ... Position Title: Recruitment and Cohort Coordinator School: NYU's School of...scalable smoking cessation package tailored specifically for the HIV clinical care context. We will be conducting respondent-driven sampling… more
- The Mount Sinai Health System (New York, NY)
- … Clinical Trials Manager, you will coordinate and manage multiple clinical trial projects and protocols, including federally funded studies, ... Administration within the Tisch Cancer Institute. **RESPONSIBILITIES** + Manages and coordinates clinical trial and related research studies conducted by the… more
- The Mount Sinai Health System (New York, NY)
- …+ Collaborates with attending physicians to identify and recruit patients eligible for clinical trial . Oversees scheduling of patient laboratory and ... to move throughout the health care system based on patient needs. **RESPONSIBILITIES** ** Clinical Practice Responsibilities:** +...of clinical program activity data. + Monitor clinical trial portfolio and enrollments to identify… more
- IQVIA (Westchester, NY)
- …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... the go-to CRO partner for visionaries whose breakthroughs may change the world, one patient at a time.** **Our team is looking for an experienced on-site CRA with**… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …and may author clinically relevant sections and review other scientific portions of clinical trial protocols and amendments + Assists with and may author/review ... process, regulatory requirements and ICH/GCP guidelines. Proven track in clinical trial process improvements. Considerable organizational awareness, including… more
- Memorial Sloan-Kettering Cancer Center (New York, NY)
- …and brings the same high level of expertise, clinical care, and access to clinical trial protocols that are available at our main campus in New York City. ... Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of… more
- Bristol Myers Squibb (Summit, NJ)
- …Articulating clinical development strategy + Analyzing, interpreting, and acting on clinical trial data to support development + Serving as principal ... in their personal lives. Read more: careers.bms.com/working-with-us . The Early Clinical Development function is part of a global scientific organization dedicated… more
- The Mount Sinai Health System (New York, NY)
- …work independently and with careful attention to detail + Experience working with clinical trial management systems including OnCore a plus + Experience working ... data, data entry, and maintenance of research databases + Recruitment of participants in clinical research studies...excellence. We share a common devotion to delivering exceptional patient care. When you join us, you become a… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …processes + Have a strong understanding of operational aspects of all phases of clinical trial conduct (start-up, conduct, close-out) In order to be considered ... patient advocacy groups), internal stakeholders (eg, Research, Early Clinical Development, Medical Affairs, Marketing, HE&OR), and internal decision boards. +… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …submissions and regulatory submissions * Accountable for timely clinical trial execution, reviewing adverse events, monitoring patient health, and quality ... The Medical Director, Clinical Sciences works with their supervisor and other...that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …and authors clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments + Authors and/or reviews documents ... We are seeking an Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development,… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …is required. * Strong understanding of operational aspects of all phases of clinical trial conduct (start-up, conduct, close-out). \#MDJOBSCD, #MDJOBS Does this ... studies and signal detection from post-marketing surveillance, with the support from Global Patient Safety. * Ensures quality of all clinical documents (eg,… more
- IQVIA (New York, NY)
- IQVIA is seeking a Senior Clinical Research Associate with at least 2 years of monitoring experience in one of the following therapeutic areas: Central Nervous ... contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH)...Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments required. + Function ... The Global Patient Safety (GPS) Lead role (Director of GPS)...PSURs, development RMPs, RMPs, etc.) and the review of clinical documents (Investigator Brochures, protocols, clinical study… more
- The Mount Sinai Health System (New York, NY)
- …provides resources/training and education, establishes workflows and tools to facilitate local trial conduct, operations, and patient recruitment . May draft ... + Identifies areas for process improvement and recommends/implements viable solutions. ** Clinical Trial Management** + Provide leadership and guidance to… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …and ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments. + Ability to work ... The Associate Director, Safety Scientist in Global Patient Safety (GPS) will play a key scientific...key scientific role in safety strategies for molecules in clinical development and post-marketing phases, under the guidance of… more
- Regeneron Pharmaceuticals (Sleepy Hollow, NY)
- …background in digital biomarker research + Proven knowledge of or experience with clinical trial development process and use of clinical technologies ... to eye trackers, you'll assess and implement these technologies, aiming to improve trial efficiency and reduce patient burden. You will champion strategic… more