- Gilead Sciences, Inc. (Foster City, CA)
- …approaches to optimize study parameters and interpret outcomes. + Prepare study protocols and coordinate execution of nonclinical studies which may involve ... responsibilities include designing and interpreting in vitro and in vivo studies , integrating data into mathematical models, and generating simulations to support… more
- Parsons Corporation (San Antonio, TX)
- …requirements. + Develop and coordinate the implementation of clinical research studies , including regulatory requirements, maintenance of study records, and ... with the collection of supporting documentation, coordinating clinical research studies , and maintaining regulatory requirements. In addition, the Research Associate… more
- Ascendis Pharma (Palo Alto, CA)
- …Associate Director ensures will be working on biostatistics deliverables, including study design, data analysis, data mining, epidemiology-related analyses, use of ... standards, specifications and datasets as needed + Contributes and reviews clinical study protocols, Case Report Forms (CRFs), and internal project plans for… more
- Battelle Memorial Institute (Columbus, OH)
- …existing solutions. Less hands-on work, more providing guidance. Serves as study director. Conducts quality control review, data reporting, workflow assessments and ... of biological systems in both simple and complex settings. Collects and studies biological data to focus on structure, function, behavior, and tailored applications.… more
- Commonwealth of Pennsylvania (PA)
- …WORK In this position, you will lead, plan, design, and conduct statistical studies and surveys. Your work will involve coordinating the Local Police Agency Contact ... Title + Credits/Clock Hours 10 WORK BEHAVIOR 2 - STUDY NEEDS AND OBJECTIVES Consult with program staff to...NEEDS AND OBJECTIVES Consult with program staff to evaluate study needs and resource and time limitations, determine appropriate… more
- ICON Clinical Research (Blue Bell, PA)
- …and logistical elements are in place for the successful execution of studies . You will contribute to the advancement of innovative treatments and therapies ... by facilitating efficient study setup processes and ensuring compliance with regulatory requirements. **What You Will Be Doing:** + Coordinating the setup of… more
- IQVIA (Manassas, VA)
- …will facilitate document flow to ensure timely completion and distribution of study documents for all clinical trials at NEXT Oncology. **Essential Duties and ... Initiation Visits and other meetings as needed + Enter study -specific information (such as but not limited to, ...Form FDA 1572s, Financial Disclosure Forms, etc.) for clinical studies being conducted at NEXT Oncology + Maintain current… more
- Adecco US, Inc. (Ocala, FL)
- …site operations process, which includes recruitment, enrollment, and retention of study participants. Essential Functions: * Conducts clinical studies according ... required to capture all data as specified by a study protocol, and for ensuring subject safety, understanding, and...for ensuring subject safety, understanding, and cooperation during the study process. Interacts with the research site team and… more
- University of Miami (Miami, FL)
- …compilation, and documentation of research data related to the assigned research studies . The incumbent also assists with the implementation of daily study ... Organizes and handles the flow of information to and from study participants, including study participant contact information. Maintains consent… more
- Vitalief (Newark, NJ)
- …provides operational and administrative support for interventional oncology clinical research studies conducted at a leading academic research center in Newark, NJ. ... and institutional requirements. + Provide operational support across the full study lifecycle, including start-up, active conduct, and close-out activities. + Assist… more