- Abbott (Abbott Park, IL)
- …and therapy areas. This individual will provide field support of clinical research study procedures with Abbott EP BU technologies, as well as, accurate technical ... Will function as an expert resource for covering clinical studies /procedures, handling challenging technical/protocol troubleshooting scenarios, critical software or… more
- Stanford University (Stanford, CA)
- …staff, researchers, outside vendors, and other staff to administer treatment and study protocols. May coordinate multi-site studies . + Develop and manage ... and maintain follow-up for children and adults in Pediatric CCT studies . We are seeking candidates with excellent communication, organization, prioritization,… more
- University of Pennsylvania (Philadelphia, PA)
- …in the coordination of clinical trials & projects. Oversees study approvals, participant enrollment & consent, visit scheduling, medication administration, ... Collaborate with Research Team and Principal Investigators to initiate study procedures for new investigator-initiated trials (IITs) and industry-sponsored clinical… more
- Beth Israel Lahey Health (Burlington, MA)
- …the study team: + Implements, conducts and coordinates assigned research studies by reviewing all pertinent study documents and assessing departmental and ... Under general supervision and direction provides direct care to research study participants and makes necessary nursing judgments. Performs diverse administrative… more
- Pfizer (Bothell, WA)
- …Oncology Biometrics** is a skilled biostatistician who can work independently as the study statistician for Phase 1-2 studies and under the direction of ... a Director of Biostatistics, or above, as the study statistician for Phase 3 studies . The person in this role: + Is an individual contributor role who… more
- Regeneron Pharmaceuticals (Warren, NJ)
- …of plans and provision of clinical operations expertise during protocol design, feasibility, study start up and conduct phases of studies . Ensure consistency ... timelines and budgets related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and company Standard… more
- Abbott (Alameda, CA)
- …is onsite in our Alameda, CA location. **What you'll work on** + Perform study site visits (SQV, SIV, IMV, COV), generate monitoring reports, and track resolution of ... clinical monitoring and site management activities, ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, Federal Regulations,… more
- University of Pennsylvania (Philadelphia, PA)
- …preparing trials for audits and inspections. The CRC will participate in study team meetings and ongoing protocol training/compliance meetings and will be expected ... the clinical trial data and records, scheduling and conducting study initiation and monitoring visits, and participating in ongoing...of the federal regulations for the conduct of clinical studies and human subject protection. + Act in lead… more
- University of Utah (Salt Lake City, UT)
- …sleep, cardiometabolic disease, and aging in diverse populations, encompassing studies that range from mechanistic to community-engaged research. Research activities ... English. This role focuses on serving as the site coordinator for a multi-site study clinical trial of insomnia treatment for midlife and older women. The position… more
- Stanford University (Stanford, CA)
- …set of multiple research protocols assuring efficiency and regulatory compliance. These studies will be conducted at the Stanford Hospital and Clinics. He/she will ... Investigators conducting clinical research. Responsibilities include preparation of initial study documents for IRB submission in compliance with all local,… more