- Cedars-Sinai (Los Angeles, CA)
- …collection/abstraction. + Enters and processes clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors. + Completes Case Report ... with local and federal guidelines. + Assists with clinical trial budgets and patient research billing. + Responsible for...Academic / Research **Job Specialty** : Research Studies/ Clin Trial **Overtime Status** : NONEXEMPT **Primary Shift** : Day… more
- Cedars-Sinai (Los Angeles, CA)
- …data collection/abstraction. Enters and processes clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors. + Completes Case ... with local and federal guidelines. + Assists with clinical trial budgets and patient billing. + Responsible for sample...Academic / Research **Job Specialty** : Research Studies/ Clin Trial **Overtime Status** : NONEXEMPT **Primary Shift** : Day… more
- Insight Global (Beachwood, OH)
- …clinical data, regulatory submissions, and medical writing. . Hands-on experience with clinical trial management systems , data analytics, and statistical tools. ... roles in MedTech or life sciences. . Deep knowledge of clinical trial design, including randomized controlled trials and regulatory standards (FDA, IRB). .… more
- Veterans Affairs, Veterans Health Administration (Charleston, SC)
- …documentation, observation and interviews with Veterans and their support systems to generate personal, vocational, and educational histories. Selects, administers, ... will be required to serve a 1 or 2-year trial period during which we will evaluate your fitness...efficiency of the Federal service. Upon completion of your trial period, your employment will be terminated unless you… more
- Takeda Pharmaceuticals (Boston, MA)
- …vendors and internal technical support groups to evaluate and optimize publications systems for reporting metrics to meet stakeholder needs + Manage medical writing ... of pharmaceutical clinical development and product life-cycle management, clinical trial design and execution, statistical methods and clinical clinical … more
- Lilly (Lebanon, IN)
- …solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental impact. The Process ... as we build a new organization, design and implement the necessary systems and business processes required to enable operational readiness, support the project… more
- Cedars-Sinai (Los Angeles, CA)
- …Case Report Forms (CRFs). + Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors. + Provides supervised patient ... with local and federal guidelines. + Assists with clinical trial budgets. + Assists with patient research billing. +...Academic / Research **Job Specialty** : Research Studies/ Clin Trial **Overtime Status** : NONEXEMPT **Primary Shift** : Day… more
- Cedars-Sinai (Los Angeles, CA)
- …and recruitment of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and supporting the informed ... objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety. + Responsible… more
- University of Rochester (Rochester, NY)
- …Improvement** + Participate in study team and sponsor meetings throughout the trial lifecycle. + Collaborate with investigators and research staff to improve site ... to national and international clinical research regulations including: FDA Clinical Trial Regulations + Office for Human Research Protections (OHRP) guidelines +… more
- Cedars-Sinai (Los Angeles, CA)
- …objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety. + Coordinates ... and recruitment of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and supporting the informed… more
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