- Cedars-Sinai (Los Angeles, CA)
- …into human diseases.** The Research Program Administrator works with the Principal Investigator or Department Head to coordinate all aspects of building a research ... **What are the Primary Duties and Responsibilities?** + With the Principal Investigator or Department Head, coordinates all aspects of building a research program… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …and assigned schedules. + Sets up experiments as prescribed by a principal investigator . + May be required to participate in laboratory maintenance activities such ... hazardous agents. + Performs related responsibilities as required by principal investigator . MINIMUM QUALIFICATIONS: + Bachelor's degree in a scientific field OR… more
- AbbVie (Mettawa, IL)
- …+ Aligns Medical education and scientific initiatives with Sci Comm Platform. Informs Investigator Initiated Study (IIS) strategy and can act as Docent for IISs. + ... + Bachelor's Degree in the sciences. Advanced Degree PhD, PharmD, PA or NP preferred . Residency or additional post doctorate experience preferred . + 5-7+ years… more
- Sanofi Group (Seattle, WA)
- …and identifying opportunities for further data collection clinical or investigator -led. + Monitors disease epidemiology and provides support, including protocol ... requested. + Responds to unsolicited requests regarding interest in Investigator -Sponsored Studies (ISS), and supports ISS submissions through appropriate internal… more
- J&J Family of Companies (Irvine, CA)
- …(eg study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports); + Ensures applicable trial registration (eg on ... Associates (CRAs); + Oversees and supports the development and execution of Investigator agreements and trial payments. + Is responsible for clinical data review… more
- Wayne State University (Detroit, MI)
- …staff with experiments/research protocols as required. Communicate with principal investigator and Postdoctoral scholars/fellows on the status of research. Collect ... and edit research data and documents to ensure accuracy. Assist principal investigator with writing methods and summarizing/organizing data to be used in preparing… more
- J&J Family of Companies (Irvine, CA)
- …- Electrophysiology division is currently seeking a **Sr.** **Clinical Research Specialist** . The preferred location is Irvine, CA on a hybrid work schedule of 2 -3 ... study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports), ensure registration on www.clinicaltrials.gov from… more
- Merck (Rahway, NJ)
- …research, post-registration company-sponsored studies and areas of interest for the investigator -initiated study program (MISP) The Sr. GDMA chairs the Global ... address life cycle management needs. Advise on areas of interest for the Investigator -Initiated Study Program. + Execute on and quickly adapt portfolio of tactics to… more
- J&J Family of Companies (Irvine, CA)
- …(eg study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports) with minimal direction. + Ensure trial registration ... and company personnel. + Lead all aspects of development and execution of Investigator agreements and trial payments. + Leads clinical data review to prepare data… more
- Wayne State University (Detroit, MI)
- …Perform scientific techniques or research protocols. Assist the Principal Investigator in designing and performing protocols. Design and perform experiments. ... needed. - Lab Tasks: Help with lab tasks as assigned by the Principal Investigator (PI). - Workshops and Classes: Participate in workshops and classes to build… more