- Lilly (Indianapolis, IN)
- …must be capable of using this expertise to enable very complex study designs driven by advanced randomization schemes, complex sourcing strategies, automated ... inventory methodologies, and data flow requirements. **Key Responsibilities:** ** Study Setup process management and oversight** + Partner with medical teams, key… more
- CSL Behring (King Of Prussia, PA)
- …+ Collaborate with Senior Managers, Clinical Finance to build and maintain robust study costing models for studies within remit, ensuring clarity around ... in partnership with Clinical Operations and POE to ensure study assumptions for all studies are up-to-date and reflect accurate assumptions for both planning… more
- 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
- 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
- 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
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