- ICON Clinical Research (Blue Bell, PA)
- Clinical Drug Supply Manager ICON plc...IP expiry. Ancillary Supplies + Develop plans for supplying clinical study sites with ancillary supplies, either ... reviews IVRS user manuals; Designs, reviews and approves IP-related study tools (for clinical study ...applies to internally sourced studies and/or CRO/Partnered studies . Collaborates and interacts with clinical trial… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- **Overview** The Sr CRA will be responsible for monitoring clinical studies at the site level ensuring adherence to protocols, timelines, ICH/GCP guidelines, and ... centralized risk-based monitoring oversight activities as assigned. * May support the Study Manager to formulate regional monitoring strategy, forecasting of… more
- ThermoFisher Scientific (Suwanee, GA)
- …Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed ... clinical research services provide end-to-end support for clinical trials from study start up to...clinical programs, minimize delays, and execute high-quality, cost-efficient clinical studies . Our Clinical Operations… more
- BeOne Medicines (Emeryville, CA)
- …with general and study -specific monitoring issues * Provide direct support to the Clinical Study Manager by assisting with monitoring visit report review ... monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with… more
- Olympus Corporation of the Americas (Westborough, MA)
- … Affairs to execute clinical strategy activities and oversee aspects of clinical studies in support of clinical evidence generation strategies across ... of Olympus's portfolio. Specifically, this individual will be responsible for writing clinical study protocols, case report forms, and study … more
- Touro University (Valhalla, NY)
- …+ Direct all aspects of research data generation and analysis including external site clinical studies and internal analytical studies . + Drive internal ... The individual will be responsible for the oversight of studies conducted out of the clinical trials...documents, patient acquisition plans, etc. + Direct establishment of clinical and analytical study related protocols and… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …not limited to, providing statistical consultation on clinical development plans, clinical trial design and clinical study endpoints, calculating sample ... Responsibilities:** + With guidance, acts as biostatistics lead on clinical studies or other non-molecule projects. +...projects and / or the statistical analysis plan and clinical study endpoints for assigned products. +… more
- Abbott (Austin, TX)
- …coding and reimbursement recommendations to support budget creation of Abbott sponsored clinical research studies . + Create study -specific reimbursement ... 500,000 people with diabetes from routine fingersticks. The **Associate Manager of Clinical Trial Reimbursement** is responsible... study reimbursement documentation for distribution to IDE clinical study sites. + Contribute to policy… more
- Kelly Services (Irvine, CA)
- **Summary:** The Senior Clinical Research Specialist will be responsible for supporting one or several clinical trials within the Clinical R&D Department ... relationships with colleagues across the organization. **Responsibilities:** + Serve as a Senior Clinical Research Specialist within the Clinical R&D… more
- Bristol Myers Squibb (Cambridge, MA)
- …and execution of multiple clinical trials (eg significant experience as a senior clinical leader), and exhibits all of the following attributes: + Able ... and achieve results through teams, and is the direct manager to Clinical Trial Physicians (CTPs) **Key...studies , with the support of the CTPs and Clinical Scientists (CS) within the asset and/or indication +… more