- Sanofi Group (Morristown, NJ)
- …responsibilities** + Produce and update clinical documents in a timely manner for study start , conduct and completion, as well as regulatory submissions ... **Job Title:** Associate Director-Principal Medical Writer **Location:** USA, Remote. Proximity...both the project as a whole, and individual clinical studies . **Our Team:** Global Medical writing and Document management… more
- IQVIA (Durham, NC)
- IQVIA is hiring a Clinical Research Associate with on-site monitoring experience in GLP-1/Obesity/Diabetes (Type II) clinical trials. Phase 1 experience is a plus! ... management work to ensure that sites are conducting the study (ies) and reporting study data as required...issues as appropriate. * Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and… more
- IQVIA (Philadelphia, PA)
- …Specifics** This sponsor-dedicated role provides country-level oversight of clinical trials from study start -up through database lock and closeout. Operating in ... visit reports, while driving risk-based mitigation plans to proactively address study challenges. The position collaborates closely with cross-functional teams to… more
- ICON Clinical Research (GA)
- …timely site activation. + Act as the main point of contact for sites, study teams, and external stakeholders throughout the start -up process. + Work closely ... As a Clinical Research Associate you will be joining the world's largest...doing?** + Works on multiple trials within Immunology - Start up focus + Collaborate with country operations teams… more
- University of Utah (Salt Lake City, UT)
- …PHS ) at the**University of Utah School of Medicine**has an opening for an Associate or Full Professor-level faculty. We seek a candidate who will serve as the ... not limited to, the following areas: (1) design and analysis of observational studies , (2) design and analysis of clinical trials, (3) causal inference, (4)… more
- University of Southern California (Los Angeles, CA)
- …with the development of regulatory and protocol materials to support clinical research studies (eg, IRB applications, study protocols, SOPs) would be a ... Postdoctoral Scholar - Research AssociateApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/Postdoctoral-Scholar Research- Associate \_REQ20164496/apply) Keck School of Medicine Los Angeles, California… more
- IQVIA (Carlsbad, CA)
- …Overview Perform monitoring and site management work to ensure that sites are conducting the study (ies) and reporting study data as required by the study ... with project needs to enhance predictability. * Administer protocol and related study training to assigned sites and establish regular lines of communication with… more
- Colorado State University (Fort Collins, CO)
- Posting Detail Information Working TitleResearch Associate I and II - Open Pool Position LocationFort Collins, CO Work LocationPosition is fully in-office/in-person ... in the top cities to live in (https://hr.colostate.edu/prospective-employees/our-community/) ! Desired Start Date Position End Date (if temporary) To ensure full… more
- Access Dubuque (Dubuque, IA)
- Associate Director of Student Access **University of Wisconsin-Platteville** 1 Positions ID: JR10003914 Posted On 09/15/2025 **Job Overview** **Position Summary:** ... The University of Wisconsin-Platteville is seeking applicants for an ** Associate Director of Student Access** . This position serves...ID 1315 Job REQ # JR10003914 \# Positions 1 Start Date 20250915 End Date 20251020 Featured Job TH… more
- University of Kansas (Lawrence, KS)
- **31346BR** **Job Title:** Administrative Associate **Department:** Bureau of Child Research **Primary Campus:** University of Kansas Lawrence Campus **Job ... - Office Management, Personnel, and Administrative Support:** The Administrative Associate will provide general administrative support to senior leadership within… more