Clinical Research Coordinator I Salary at Macro Trials BETA

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 Position Summary: The Clinical Research Coordinator undertakes the performance of clinical trials. The individual seeking this position will be responsible for all aspects of completion of the research study. Ideal candidate will possess outstanding organization, communication skills, and an ability to adjust and interact with various types of people. Must be a team player, maintain confidentiality, and be comfortable working in the medical field. Candidate will demonstrate customer service that is compassionate, courteous, friendly, non-judgmental, and demonstrate a respect for privacy. Location: Fullerton, CA Work Schedule: Monday through Friday: 8:00 am - 5:00 pm, additional hours as necessary. Education: Some college experience required. Bachelor’s degree preferred but not required. Experience: Must have a minimum of 6 months of experience in clinical research. Preference given for individuals who have more than 12 months experience in the above fiel

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** **Join Cedars-Sinai and become part of a team that is at the forefront of medical advancements!** Work alongside physician-scientists and researchers who are making life-saving medical and scientific breakthroughs. Our team of scientists develop some of the most advanced clinical trials in the world. The Clinical Research Coordinator I will work independently providing study coordination, screening of patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. This position is responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. The incumbent will be responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. The CRC I member will present study information at research staff meetings and ensur

Our client, a Medical Center facility under the aegis of a California Public Ivy university and one of largest health delivery systems in California, seeks an accomplished Clinical Research Coordinator. _______________________________________________ NOTE- THIS IS 100% ONSITE ROLE & ONLY W2 CANDIDATES NO C2C/1099 *** Candidate must be authorized to work in USA without requiring sponsorship *** Position: Clinical Research Coordinator (Job Id - # 2808451) Location: Los Angeles CA 90024 Duration:6 Months + Strong Possibility of Extension ______________________________________________________ Job Title: Clinical Research Coordinator SHIFT: 5x8, DAYS 8:00am to 5:00pm. EXPERIENCE: The CRA will be responsible for ensuring protocol procedures are completed accurately, safely, and in a timely manner, this includes responsibility for research assessment and patient intervention under the supervision of the Principal Investigator. Additional responsibilities include regulatory compliance, patient

Opportunity to join a growing Clinical Research Site Network within the Northridge area of Los Angeles! Great opportunity for experienced Clinical Research Coordinators or Research Assistants. Bilingual in Spanish is a plus! Highlights Play a major role in cutting-edge clinical trials - a meaningful healthcare position! Full Benefits (Health, Dental, Vision, 401k w/ 4% Match, PTO, Paid Holidays) Gain experience in the fast-growing world of clinical research and develop skills that are in high-demand Monday - Friday 8am-5pm Position To coordinate a variety of complex activities and perform duties and procedures related to the start-up, conduct and close-out phases of clinical pharmaceutical and device research protocols. Obtain clean, objective, and accurate data within sponsor timelines while following applicable SOPs, policies and procedures, federal regulations, medical ethics, Good Clinical Practices (GCPs), International Council of Harmonization (ICH), Institutional Review Board (I

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 Are you interested in working in clinical research? Do you have a background in nursing or life sciences and are interested in bringing innovation to your community? Do you want to use your strong organizational skills to help others? If so, a position as a clinical research coordinator might be the fit for you. Clinical Research Coordinators conducting studies in a private, ophthalmology practice is a position that allows ongoing growth and development. As an clinical research coordinator, you’ll assist principal investigators in recruiting and management research studies directly affecting the eyecare industry. Join Visionary Eye Institute to grow in this exciting position and start your new career! Visionary Eye Institute was founded by Dr. Ehsan Sadri in 2019 to advocate for all communities by providing innovative and life-changing eyecare. Our practice specializes in medical eyecare and surgery, and we also have a clinical research division that all