Researcher Salary at Variety Sa BETA

What Makes a Honda, is Who makes a Honda Honda has a clear vision for the future, and it’s a joyful one. We are looking for individuals with the skills, courage, persistence, and dreams that will help us reach our future-focused goals. At our core is innovation. Honda is constantly innovating and developing solutions to drive our business with record success. We strive to be a company that serves as a source of “power” that supports people around the world who are trying to do things based on their own initiative and that helps people expand their own potential. To this end, Honda strives to realize “the joy and freedom of mobility” by developing new technologies and an innovative approach to achieve a “zero environmental footprint.” We are looking for qualified individuals with diverse backgrounds, experiences, continuous improvement values, and a strong work ethic to join our team. If your goals and values align with Honda’s, we want you to join our team to Bring the Future! Job Purp

Eyeline Studios At Eyeline, Scanline VFX's virtual production division, we want to provide you with a solid foundation where you can be a part of an innovative team of brilliant researchers, developers and virtual storytellers. Learn more. As a Research Scientist, you will develop new technologies to revolutionize live-action content creation and storytelling. You will conduct applied research in computer vision and computer graphics leveraging Machine Learning. The primary objective of this position is to empower storytellers worldwide by creating innovative tools and algorithms that enhance virtual production, visual effects (VFX), and post-production. By leveraging your expertise, you will enable artists to concentrate on the creative aspects of their work while leveraging the most powerful tools to achieve their vision. Collaboration with content production teams, product management, and engineering teams will be crucial in order to develop and test novel models and algorithms. Key

Job Details Level Experienced Job Location Los Angeles Office - Los Angeles, CA Description Buchalter APC has an opening for a Research Analyst within our Research & Information Services Department. The Research Analyst conducts in-depth reference and research across various practice areas of law and business, and supports the Firm's business development efforts. The ideal candidate thrives in a fast-paced environment, is committed to excellence in the workplace, and is forward-thinking, proactive, analytical and a confident individual with impeccable research skills, business acumen and acute attention to detail. This position requires proficiency in prioritizing and completing multiple projects with varying deadlines and levels of difficulty. The candidate should possess a keen interest in innovation and technology, and ability to learn new legal and business research platforms. This position can be based in any of the following offices: Los Angeles, Sacramento, Salt Lake City, San D

Job Description Job Description We are seeking an energetic Clinical Research Coordinator (CRC) to join our team. The CRC is responsible for the coordination and administration of clinical trials under the direction of the Principal Investigator and Scientific Director. The CRC will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials. The CRC will perform diverse administrative duties requiring a high level of knowledge of study specific protocols, as well as coordination and collaboration with research colleagues and departments. Duties and Responsibilities Perform study procedures in accordance with GCP and study protocols Coordinate protocol related research procedures, study visits, and follow-up care Organize and maintain paper and electronic study data in a complete and correct manner Work closely with recruitment and pre-screening teams to meet study enrollment goals Adhere to an IRB approved protocol Partici

Job Description Job Description National Institute of Clinical Research, a research organization serving the pharmaceutical and biotech industries, is searching for a Clinical Research Coordinator with 2 or more years of experience. Duties for this position will include managing the study from placement to completion of the final study report. The CRC is responsible for the conduct of quality and efficient clinical trials. REQUIREMENTS: A minimum of 2 years of clinical research experience is preferred. In-depth knowledge of the clinical research process, including Good Clinical Practices and ICH guidelines; Strong interpersonal and communication skills; excellent attention to detail; exceptional organizational and planning skills. Able to project and coordinate study needs in advance. Candidate needs to have good troubleshooting and conflict-resolution skills. Being bilingual in English/Spanish is a plus! NICR is an independent, multi-site clinical trial management organization (SMO).

Job Description Job Description We are seeking a Market Researcher to join our team! You will be responsible for gathering and analyzing key market information, as well as identifying areas of improvement to increase company revenue and brand. Responsibilities: Conduct market research to determine potential of products and services Perform analysis of market strengths, weaknesses, opportunities and threats Development and implement innovative marketing campaigns Translate complex data into simple graphs and text Compile and present data for other departments Qualifications: Previous experience in market research or other related fields Familiarity with quantitative and qualitative data collection Strong analytical and critical thinking skills Strong communication and presentation skills Ability to work well in teams

Job Description Job Description We are seeking a Clinical Research Coordinator to join our team! This role establishes and executes all logistics related to a variety of clinical research projects - including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety. The successful candidate will coordinate all administrative functions for research studies, including scheduling of patients for research visits, procedures and labs and completion and maintenance of consent forms, case report forms, SAE’s and source documents. Responsibilities: Responsible for screening and recruitment of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and supporting the informed consent process. Responsible for accurate and timely data collection, documentation, entry and reporting, including resolution of queries from sponsors or regulatory entities. Coordinates institutional

Job Description Job Description About us www.bayviewresearch.com Bayview Research Group, LLC - A Clinical Research Site Clinical Research Assistant's Role and Responsibilities: Schedule study participant's visits and complete study procedures including phlebotomy, sample processing & shipping, vital signs, medical history, collection medication history, etc. Responsible for accurate and timely data collection, documentation, entry, and reporting with quick response times to data queries Maintain accurate source documents related to all research procedures Responsible for all filings including reports or source documents going to the subject's binder. Maintain research practices using Good Clinical Practice (GCP) Guidelines Maintain strict patient confidentiality according to HIPAA regulations and applicable law Participate in required training and education programs Ensure that all study communication is consistently documented and communicated to appropriate team members promptly per