- Rush University Medical Center (Chicago, IL)
- …study protocols. **Responsibilities:** * Coordinates aspects of less complex research studies including, but not limited to, study start-up, initiation ... proposals. * May act as lead for less experienced Research Assistants, work - study students, interns and volunteers including orientation, training, and providing… more
- Astellas Pharma (Northbrook, IL)
- …observational studies + Write, review, or contribute to key study documents to ensure optimal methodological & statistical presentation. These documents include, ... If you want to be part of this exciting work , you belong at Astellas! Astellas Pharma Inc. is...analytic researcher informing and conducting Real World Data (RWD) studies at any time in the drug lifecycle. You… more
- Genentech (South San Francisco, CA)
- …Management to enable data-driven decision-making from first-in-human through proof-of-concept studies . As trusted partners in early development, we design efficient ... for ensuring data quality, integrity, and readiness across multiple studies , partnering closely with Biostatistics, Data Science, Clinical Operations, and… more
- Takeda Pharmaceuticals (Boston, MA)
- …do this, we empower our people to realize their potential through life-changing work . Certified as a Global Top Employer, we offer stimulating careers, encourage ... Development Plan (IGDP). Responsible for review of synopses, other relevant clinical study documents and critical Study Results. Provide leadership and oversight… more
- University of Utah (Salt Lake City, UT)
- …clinical research studies ; and (3) assist the Principal Investigator and study team in achieving study integrity and objectives through the successful ... **Full Time or Part Time?** Full Time **Shift** Day ** Work Schedule Summary** **VP Area** U of U Health...**Responsibilities** 1. Screen and recruit participants for clinical research studies . 2. Fully understand the informed consent process and… more
- Cedars-Sinai (Los Angeles, CA)
- …and leading staff. + Provides guidance, instruction and expertise to team members on study requirements and clinical coordination of the studies . + May assist ... This is an **on-site role** with a **4/10 schedule** , offering a great work -life balance. If you hold an **active RN license in California** and have **prior… more
- University of Miami (Miami, FL)
- …planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies . This role assists in the day-to-day operations of clinical ... research protocol implementation, and carries out study coordination duties from protocol initiation to study close-out according to regulatory/sponsor… more
- University of Miami (Miami, FL)
- …procedures according to the protocol. + Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, ... according to protocol requirements. + Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines,… more
- Rush University Medical Center (Chicago, IL)
- …Rush Medical Center Hospital: Rush University Medical Center Department: Cancer Center-Res Fac ** Work Type:** Full Time (Total FTE 1.0) **Shift:** Shift 1 ** Work ... clinical care to research participants while supporting the conduct of clinical studies under the direction of a Principal Investigator (PI). Working as part… more
- Fresenius Medical Center (Tupelo, MS)
- …personal computer work and interaction with patients, field staff, physicians and study sponsors. + The work environment is characteristic of a health care ... for the collection and submission of regulatory documents, performance of study specific procedures, regulatory reporting requirements as instructed by the PI… more